Many claims are being made about what one can do with Live Blood Analysis and this course will blow the trumpet of caution on several popular assumptions. That way you are going to end up with 1) a balanced view and 2) greater clinical confidence. By examining this topic in an comparative way from several angles you will get an excellent grasp of what is reasonable and above all what works in clinical practice!!
Monday, August 18, 2008
Yeast Causing Cancer? Part 2
Yeast Causing Cancer?
Sunday, August 10, 2008
Balancing the pH is a major step toward well-being and greater health.
An acidic pH can occur from, an acid forming diet, emotional stress, toxic overload, and/or immune reactions or any process that deprives the cells of oxygen and other nutrients. The body will try to compensate for acidic pH by using alkaline minerals. If the diet does not contain enough minerals to compensate, a build up of acids in the cells will occur.
An acidic balance will: decrease the body's ability to absorb minerals and other nutrients, decrease the energy production in the cells, decrease it's ability to repair damaged cells, decrease it's ability to detoxify heavy metals, make tumor cells thrive, and make it more susceptible to fatigue and illness. A blood pH of 6.9, which is only slightly acidic, can induce coma and death.
The reason acidosis is more common in our society is mostly due to the typical American diet, which is far too high in acid producing animal products like meat, eggs and dairy, and far too low in alkaline producing foods like fresh vegetables. Additionally, we eat acid producing processed foods like white flour and sugar and drink acid producing beverages like coffee and soft drinks. We use too many drugs, which are acid forming; and we use artificial chemical sweetners like NutraSweet, Spoonful, Sweet 'N Low, Equal, or Aspartame, which are poison and extremely acid forming. One of the best things we can do to correct an overly acid body is to clean up the diet and lifestyle.
To maintain health, the diet should consist of 60% alkaline forming foods and 40% acid forming foods. To restore health, the diet should consist of 80% alkaline forming foods and 20% acid forming foods.
Generally, alkaline forming foods include: most fruits, green vegetables, peas, beans, lentils, spices, herbs and seasonings, and seeds and nuts.
Generally, acid forming foods include: meat, fish, poultry, eggs, grains, and legumes. Continue Reading >>
Thursday, July 24, 2008
Red Meat Linked to Breast Cancer
They found that women who ate more than 1 1/2 servings a day of beef, lamb, or pork had nearly double the risk of hormone-receptor-positive breast cancer than those who ate three or fewer servings per week.
The researchers theorize that factors including carcinogens found in cooked or processed red meat and growth hormones given to cattle may contribute to the higher rate of breast cancer incidence.
In my own research, I have found that eating meat increases acidic residues of nitric, uric, phosphuric and sulphuric acid that will also increase your risk for breast cancer. Acidic breasts are cancerous breast.
Eliminate the acid and you will reduce your risk for breast cancer.
So, if you want to prevent or reverse breast cancer then you must reduce your acidity by eliminating all animal meat from your diet.
The cure for cancerous breasts will not be found in its treatment of the tissues but will be found in its prevention of acidic residues from acidic foods like meat, milk, cheese and yogurt.
More informations here:
- Live_blood Analysis
- Live_Blood_Analysis Darkfield Microscopy Courses
- dark field microscopy
- pleomorphism
- Günther Enderlein
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Monday, June 09, 2008
How the Body Works : The Small Intestine
Tuesday, June 03, 2008
Friday, May 02, 2008
The Acid Nicotine In Tabacco and Chewing Gums Posion White Blood Cells
The acid nicotine, a component of tobacco smoke and chewing gums, can make the body more prone to out-fections and inflammation, a research team has found.The study, published in Cell Biology, was led by David Scott, a University of Louisville oral health researcher.
Scott's team found that nicotine affects the production of one type of white blood cells, one of the body's primary defenses against infection and dis-ease.
White blood cells are produced out of red blood cells and body cells and the cells mobilize in the bloodstream to maintain cleanliness in the blood plasma and interstial fluids of bacteria and yeast. The researchers learned that white bllod cells tainted with nicotine were less able to mobilize in order to collect bacteria and yeast than white blood cells not exposed to the acid nicotine.
The researchers determined that the acid nicotine suppresses an important cell function that helps mediate bacteria and yeast and, at the same time, increases levels of exotoxins and myctotoxins (acidic waste products from bacteria and yeast) that promote the biological transformation of healthy body cells and tissues.
"Both of these findings partially explain chronic tobacco users' increased susceptibility to bacterial infection and inflammatory diseases," said Scott.
Although nicotine has been known to affect the immune response, this is the first study to examine how nicotine affects production of bacteria-collecting cells in the bone marrow and their mobilization into the bloodstream.
According to Dr. Robert O. Young, a research scientist at the pH Miracle Living Center, "the acid nicotine from tobacco or nicotine chewing gums will poison and paralyze the white blood cells for up to five hours.
When white blood cells are poisoned and paralyzed they cannot perform their normal activity of helping to maintain fluid purity and alkalinity. This can then cause increased acidic cellular debris in the body fluids causing blood and lymphatic congestion leading to poor circulation, light headedness, dizziness, cold hands, cold feet, irritation, and inflammation.
If the white cells are suppressed on a regular basis by continued use of nicotine containing products this may lead to more serious acidic symptomologies such as ulceration and degeneration of the tissues and organs leading to heart dis-ease and cancerous conditions."
Saturday, April 19, 2008
The Key To Health, Energy and Fitness
The nation's 10 most expensive dietary and metabolic acid caused medical conditions cost about $500 billion to treat in 2005, according to the latest News and Numbers from the Agency for Healthcare Research and Quality. The money paid for visits to doctor's offices, clinics and emergency departments, hospital stays, home health care and prescription medicines.Estimated spending for the 10 most expensive acid conditions are:
* Heart conditions $76 billion
* Trauma disorders $72 billion
* Cancer $70 billion
* Mental disorders, including depression $56.0 billion
* Asthma and chronic obstructive pulmonary disease
$54 billion
* High blood pressure $42 billion
* Type 2 diabetes $34 billion
* Osteoarthritis and other joint diseases
$34 billion
* Back problems $32 billion
AHRQ, which is part of the U.S. Department of Health and Human Services, works to enhance the quality, safety, efficiency, and effectiveness of health care in the United States. The data in this AHRQ News and Numbers summary are taken from the Medical Expenditure Panel Survey, a detailed source of information on the health services used by Americans, the frequency with which they are used, the cost of those services, and how they are paid.
We have more medicine and health care then any where in the world and yet rank number 37 in over all health as a people.
It is my personal belief that we as a Nation we need more education not medication!
I personally believe that lifestyle and dietary choice determines the quality and quantity of life. Sickness and disease and health and fitness is not something that you get it is something that you do with your daily lifestyle and dietary choices.
The pH Miracle Lifestyle and Diet can
eliminate most if not all dis-ease off the planet.
It is based upon a scientific principle that the human body is alkaline by design and acidic by function.
The key to health, energy and fitness is to maintain the alkaline design of the body through an alkaline lifestyle and diet.
Tuesday, March 25, 2008
No More Heart Attacks or Strokes
Unlike most medical doctors, natural healers do not look to pharmaceutical companies as their first line of defense against heart disease. Instead, they turn to natural means of lowering risk.
If a patient has angina caused by acid bound cholesterol forming blockages to the heart, a cardiologist might use angioplasty to compress or remove the blockages, and prescribe a statin drug to lower cholesterol.
But in addition to the risks involved in the procedure itself, results are often temporary and the blockages return in a few short months because the main cause of the blockage has not been dealt with - dietary and metabolic acid. Acidic Statins also cause stage 4 acidic side effects, including severe muscle pain or weakness and sleep disturbances.
A natural healer would prescribe lifestyle and dietary changes to restore blood flow to the heart by naturally lowering acid bound cholesterol and decreasing acidic artery-clogging deposits. Below are the steps that a pH Miracle Life Coach might use to lower acidity and thus lower cholesterol levels to protect the body from heart attacks and strokes. I refer to this plan as the C.O.W.S. Plan which is an acronym which stands for a lifestyle and diet of chlorophyll, oil, oxygen, water, salt and sunshine. To be truly healthy you need to start eating like COWS.
1) Chlorophyll - A diet high in green vegetables and green fruits. I also recommend fresh green juices and liquid chlorophyll in alkaline water everyday. You can add the liquid chlorophyll to your green juices or green powders. A man, woman or child should drink at least 1 liter of green drink for every 25 kilos of weight or 50 pounds. I have created the first liquid chlorophyll fresh from alfalfa grass, without alcohol, chemicals or sugars that can be added to water, green drinks and green shakes. You can order this liquid green by calling 760-751-8321. It comes in a 4 ounce bottle and is 100% pure and organic.
2) Oil - I recommend at least 2 to 3 ounces or 100 to 150 mL of cold pressed omega 1, 3, 5, 6, and 9 oils.
My favorite is the avocado oil and the pomagranate oil.
I also recommend flax, hemp, pumpkin, olive, primrose.
sesame and borage oil.
3) Oxygen - The best way to increase oxygen is through exercise. The second best way to increase oxygen is with sodium, magnesium, potassium,calcium bicarbonate, and potassium hydroxide.
4) Water - The single most important thing that one can do is to drink more 9.5 alkaline pH water and at least 1 liter per 24 kilos of weight or 50 pounds.
The best drinking water is purified, alkalinize, and energized. You can learn more about the right kind of water to drink by going to our website at:
5) Salt - Without salt there would be no life. Salt is the catalyst of electron transport. It is what keeps your heart beating and energy flowing to every anatomical element that makes up every cell. I recommend eating at least 1 gram of salt for every
5 kilos or 10 pounds of weight. The best salt in the world is whole, unprocessed sea salts in a colloidal form. Such a salt exists and is called pHlavor by Young pHorever.
6) Sunshine - Just like salt without sunshine all life on earth would cease to exist. I recommend at least
1 hour of daily exercise and the best way to get 1 hour of exercise is while you are walking, jogging, bicycling, swimming, running, playing tennis, rebounding, etc. outside in the sun. The sun releases photons which the body converts into electrical energy via the eyes and skin. This is a natural and effective way to energize the body.
The following are some additional ways to help keep your body and heart healthy from dietary and metabolic acids:
1) High fiber diet - A daily high-fiber intake would include five to ten grams of soluble fiber. This also helps to keep the bowel clear of undigested food and acidic toxins which are adsorbed and absorbed by the fiber. I would also recommend magnesium oxide with sodium bicarbonate in a product I call pHlush.
2) Co-Q-10 - Research has indicated that taking Co-Q-10 everyday may help to prevent heart attacks and strokes.
3) Nuts - All nuts, but especially walnuts and almonds, contain heart-healthy omega-3 fatty acids, vitamin E and soluble fiber. Studies have shown that people who eat nuts twice a week lower their risk of heart disease by 30 to 40 percent.
4) Plant Sterols - Sterols, which are found naturally in many plant foods, decrease the amount of acidic bound cholesterol absorbed by the body. The most important and the most powerful plant sterol of comes from green fruits and vegetables, such as avocado and broccoli.
5) Glutathione - the most powerful antioxidant for buffering dietary and metabolic acids that can make your heart weak. I would suggest 1 to 2 teaspoons of liquid glutathione every day to keep your heart and body healthy and strong.
Dr. Robert O. Young
Monday, March 17, 2008
No More Type I or Type II Diabetes!
The story begins two months ago with a 6 year old child named Gabriel who was diagnosed with onset Type I Diabetes. Through Gabriel's parents I had the honor to meet and work with Gabriel to help him reverse this condition.
When I looked at Gabriel's live and dried blood he had all the markers for the condition he had been diagnosed with by his doctor - Type I diabetes.
The blood showed:
1) White spots on the red blood cells,
2) Targets in the center of the red blood cells,
3) Yeast cells, like candida in the blood plasma, and
4) A dark protein ring in the center of the coagulated blood, indicating bowel congestion.
I shared with Gabriel and his parents that diabetes starts in the bowel not in the pancreas. Balancing blood sugars has everything to do with restoring the alkaline pH of the small and large intestines by eliminating the congestion of undigested chicken, beef, pork and fish. I helped them understand that the major cause of diabetes in children is from protein not from sugar. I knew if Gabriel would clear his bowels of undigested animal proteins his blood sugars would normalize and "No More Diabetes!"
This is exactly what happened - Gabriel cleared his bowels and now has normal blood sugars and "No More Type I Diabetes!"
The following is Gabriel's story as told by his incredible Mother who had the insight and inspiration to look outside the medical box of current medical thought.
Dear Dr. Young,
Two months ago my husband and I were shocked when our family doctor informed us he thought our six year old son, Gabriel, had Type 1 Diabetes. The pediatric endocrinologist we were referred to was reasonably sure he had the disease .Although the specialist said we detected it early, he estimated that Gabriel would be insulin-dependent within six months. When we asked if there was anything we could do, the doctor assured us there was no way to prevent the onset of Type 1 Diabetes. We would just have to wait for the disease to run its course.
Our hearts were grieving for our precious son.
We immediately began learning all we could about Type 1 Diabetes. I am an R.N., and I have studied health alternatives and nutrition. I began scouring the internet and researching sources I have studied.
After considering many possibilities, Dr. Youngs's research seemed the most promising. Dr Young generously invited us to visit the research center as a case study for his microscopy course. He confirmed the Type 1 Diabetes diagnosis and started Gabriel on the pH Miracle Living Plan or the COWS Plan as outlined in his book, The pH Miracle for Diabetes.
The day we visited the pH Miracle Center, Gabriel began drinking what he calls "green power". We began the alkaline diet immediately. His blood sugar levels dropped to within normal range and have remained normal. Gabriel says he feels so much better. Overall, his flagging energy has returned to its previous vitality.
Gabriel now tells everyone he wants to be a doctor.
He wants to help other sick people like Dr. Young.
We thank God for the pH Miracle Living program which has been and answer to our prayers. Thanks to Dr.
Young's dedicated research, our mourning has been transformed into hope.
Gabriel's Mom
The key to reversing Type I diabetes is the healing of the small intestine and the intestinal villi or root system of the body. When we have a healthy small intestine we can build healthy red blood cells which can then build a healthy body.
Very few people realize that sugar is a waste product of cellular degeneration or breakdown, not a fuel for energy. Think about it for a moment when you consider a banana as it ripens or ferments - it becomes sweeter with the acid sugar - it is melting into sugar.
This is what is happening to the person doing diabetes.
He or she is melting into sugar.
When we clear the bowels of protein and begin to build blood with chlorophyll, oil, alkaline water and salt we can expect only one thing - incredible health and energy and "No More Diabetes!"
In fact, if more people understood the principals I teach there would be "No More Diabetes" of any type in the world today!"
Wednesday, March 12, 2008
Weight-Bearing Low Impact Exercising
A Duke University Medical center report on the various factors that affect weight loss points to vigorous, sustained exercise as a key factor.Estimates for the benefits of milder forms of exercise, such as a one-mile walk are imprecise at best, and often do not take into account factors that reduce their actual effectiveness.
Machines such as treadmills, for example, overestimate the amount of acids eliminated by 10-15 percent.
However, weight-bearing, gravity-fighting, low impact exercises like rebounding, isotonic weight lifting, dancing, skating, running, stair-climbing and whole body vibrational exercising eliminates the same amount of metabolic acids, in the same period of time, than gentler water-based exercises or cycling, although some make up for this by cycling for longer periods.
How skillfully you perform your personal exercise regimen affects the amount of acids you eliminate through the sweat glands. Poor technique may make you work harder and create more acid than you are eliminating and you'll quit faster and may hurt yourself along the way.
References:
New York Times September 12, 2006
Rocky Mountain News September 19, 2006
Friday, March 07, 2008
Testing Urine and Saliva pH
We are receiving many questions on howto best monitor the pH of the saliva and urine.
Here is how to test your own pH..........
The pH Miracle Living Acid/Alkaline Saliva and Urine Test:
1. First, upon waking test your saliva with the pHydrion paper. When you get out of bed, lick and wet the end of a pHydrion test strip with your saliva. Note the color change and write down the pH number.
Do this before brushing your teeth, drinking, smoking, or even thinking of eating any food.
The optimum saliva pH should be 7.2.
2. Next, test your first urine of the morning.
This is urine that has been stored in your bladder during the night that is ready to be eliminated when you get up. You need to pee on a strip of pHydrion paper, note the color change and write down the pH number.
The first urine should run optimally at 7.2 of greater.
If your first urine pH is lower than 7.2 you are deficient in alkaline buffers and need to move to a more alkaline diet rich in fresh green vegetables and fruits. If your first urine pH is higher than 7.2 your alkaline buffers are sufficient to neutralize the acidic foods and drinks you ingested the day before.
To increase urine pH which is a direct indicator of tissue pH take 3 tsp. of pHour salts in 4 to
6 ounces of purified water.
To balance the pH of the urine you need to move away from acidic foods and drinks and begin ingesting liberal amounts of electron rich green vegetables, low sugar fruits and healthy polyunsaturated fats. I call this way of eating and drinking the cows program which stands for chlorophyll, oil/oxygen, water and salts.
3. Next, test your second morning urine before eating any food. This number should be the pH of your second urine after you have eliminated the acid load from the day before.
The acids should be gone the second time you go to the bathroom so your urine pH should be ideally 7.2 or higher.
If the pH is lower than 7.2 then you are in a state of latent tissue acidosis and you are deficient in alkaline buffers such as sodium, potassium, magnesium and calcium bicarbonate.
The lower pH is also indicative of a diet high in protein and an increase in acids from proteins including nitric, sulfuric, phosphoric and uric acids. Eliminate from the diet proteins from beef, chicken, turkey, pork and fish to normalize pH at 7.2 while eating liberal amounts of green foods and green drinks, healthy polyunsaturated fats and alkaline mineral salts, like pHour salts.
4. For breakfast eat an avocado soup, vegetable soup, the healing soup or drink some fresh almond milk or a fresh green drink. Wait five minutes and then check your urine and saliva again. Write these pH numbers down also. The pH numbers will go up from the first and second morning urine and saliva if you have sufficient alkaline reserves to buffer acids. If you do not then the pH numbers will show very little change or even go down from the early morning pH numbers.
5. Make sure you check your urine and saliva pH between meals, i.e., between breakfast and lunch and between lunch and dinner. The pH should always be between
7.2 to 8.4, right after meals and 7.2 a couple of hours after meals.
The five tests above show the following:
1. The efficiency of the digestive or alkaline buffering system to deal with what you ate the night before, i.e., the first and second AM urine and saliva pH.
These numbers will change from day to day if you are living an eating acidic. When you begin The pH Miracle Living Plan and start eating the COWS Plan you will see the pH of the urine and saliva become more constant and balanced at a pH of 7.2 or higher.
2. How well you treat yourself in general, i.e., how 'strong'
the salivary glands, stomach, pancreas, gallbladder and liver are in dealing with excess acidity. This is once again the AM urine and saliva pH. This number shows the overall state of your health, the condition of the alkaline reserve of your body which reflects the diet you have been eating over the last months and years.
This pH number stays rather constant and will only change after some work has been done in alkalizing and energizing the body as outlined in the pH Miracle books. Since the saliva and urine pH is an indicator of extracellular and interstitial pH, saliva and urine pH readings should never be below the pH of the sodium bicarbonate buffer system, 7.2. (See below).
The most accurate readings of saliva and urine pH is recorded immediately upon awakening--after sleeping at least five hours and before brushing your teeth.
It is during sleep that the body removes waste and is in an anabolic state restoring and replenishing the body.
For example, if you have a saliva or urine pH of 5.5 and only 5.6 after eating, you know that you are deficient in alkaline reserve and your body is devoid of the minerals necessary to process food properly -- your body cannot adequately respond to the physiological crisis of handling food or drink that is acidic.
3. The pH of your saliva and urine after you eat or drink gives you an indication of your alkaline mineral reserves and your body's ability to deal with the acid residues created from the digestion of that food or drink. It is normal for your pH number to increase after you eat or drink not stay static or decrease.
This once again indicates your inability to deal with acid, the deficiency of alkaline reserves and the buildup of latent tissue acidosis.
Even if you think of a food like an avocado or a lemon the pH of your saliva should increase by a whole point or ten times. This simple test indicates you have sufficient alkaline reserve minerals to pull into your alimentary canal to begin the alkaline buffering process.
The ideal urine and saliva pH pattern is 7.2 on awakening, 7.2 before eating and 7.2 to 8.5 following any alkaline meal or drink.
A simple test can be done at most any time of the day by eating a few almonds.
This will check the adequacy of the alkaline reserve of the body. When a healthy person with adequate alkaline reserves eats a few almonds, the saliva pH almost immediately goes up to a pH of 8.4.
The more acidic the food that is eaten, the more rapid the response of the alkaline reserve, and the higher the saliva pH should be following a meal.
4. The pH of the saliva and urine between meals should be kept in the basic range, pH 7.2 or higher.
After one eats, the stomach releases its necessary sodium bicarbonate to help alkalize the food. While doing this, it makes an equivalent amount of base or baking soda, sodium bicarbonate, that is picked up by the blood stream and delivered to the alkaline glands of the body, the saliva, the pancreas, the gallbladder, the pylorus glands in the stomach and the liver. The maximum amount of base in the blood and therefore in the urine and saliva occurs one to two hours after you eat.
This rhythm of the acid and base flow of the body is called by Frederick F. Sander, the Base-floods and the Base-tides of the Acid-Base household.
This information was first published in 1930, by Frederick F. Sander, a German scientist, in a book called, The Acid-Base Household of the Human Organism and its cooperation with the nail circulation and the rhythm of the Liver.
In his book he states that the body fluids and therefore the urine is most acid at 2:00 A.M.
(pH 5.0 to 6.8) in the morning (the base tide) and most alkaline at 2:00 P.M. (pH 7.0 to 8.5) in the afternoon (base flood).
'The ideal pH numbers depend on the time of day.
Plotted on a curve it looks like the double hump of the back of a camel. Two times a day the urine should be alkaline and that is the top of the humps and corresponds to 10 A.M. and 2 P.M., the alkaline tide after meals. During the rest of the day the pH should be between 6.8 and 7.2. This is optimal urine. The first urine in the morning should be more acidic because of the decalcification that takes place during the night in neutralizing excess acids.'
If all the acids generated in a day from digestion, respiration, metabolism, degeneration, emotions, and toxic environments are not all flushed out during the night they accumulate, day after day. The results are the expression of states of imbalance as the body desperately tries to maintain the alkaline fluid pH at 7.365. The day to day buildup of acids affects each of us differently depending on our genetics, lifestyle and diet.
I have found that acids settle in the weakest parts of the body and if not eliminated through the bowels, urinary system, lungs or skin, acids are then bound to fat and stored on our hips, thighs, stomach, breasts and brain. Bottom-line acids are the expression of all symptomologies and the direct cause of ALL sickness and disease.
Monitoring your saliva and urine pH puts the responsibility of caring for your health back into your hands. Measuring the saliva and urine pH guides your therapy and shows you how living, eating and drinking determines the quality and quantity of your life.
You should monitor your saliva and urine each day for at least 12 weeks or until you establish your balanced pH at 7.2. Once you have established a balanced saliva and urine pH at 7.2 or higher you can reduce the number of tests to once a day or
2 to 3 times a week.
Saturday, March 01, 2008
The history of the Monomorphismus and Pleomorphismus
The history of the Monomorphismus and Pleomorphismus
Approximately around 1898 a controversy among the scientists over the kind, the nature and the behavior of the bacteria began. Up to then one knew the spleen fire exciters, the Cholera germ, the Diphtheria, typhoid fever, Tuberculoses and the Syphilis germ.
Mainly two thinking directions took the true nature up of the bacteria for itself to know. Some stated, bacteria are not capable of changing their appearance; the other stated the opposite: the fact that under certain conditions bacteria quite change and/or another shape to accept and develop themselves further can.
The first group were the Monomorphist (of griech. monomorph - one form), the second group were the Pleomorphist (of griech. pleomorph - many forms).
Louis Pasteur (1822-1895) was a Monomorphist, on its dying bed however explained it the important sentence:THE ENVIRONMENT IS NOT EVERYTHING THE MICROBE IS ANYTHING .It professed itself to the Pleomorphismus.
Founder of the Pleomorphismus was the Frenchman Antoine Bechamp. Since then we have to do it with a constant change of the micro organisms: not ill-making the only by antibiotics and all chemical weapons since then against, but also against the physiologically good (healthy-holding) bacteria to be used, the micro organisms constantly develop themselves further into higher valence forms (ill-making forms); indeed in viruses, bacteria and mushrooms.
The fighting medicine tries to fight and defeat the cancer for over 100 years. "as the victory from....?" sees
By epidemics, e.g. AIDS and SARS, clearly shown us that viruses always develop themselves further into newer and more aggressive manifestations.
Fight always produces a fight. We hear to nevertheless finally fight on!
LOVE is the largest STRENGTH in the COSMOS.
Only by the holistic viewpoint, the CYCLOGENY (CYCLOS means CIRCLE, gene OS birth), we can use natural cures modulator. These modulators know under certain conditions the degenerate micro organisms viruses, bacteria, mushroom again into the prototype, which Endobiont, back to bring.
Monomorphist starting points are: linear
Pleomorphist starting points are: three-dimensional
Holistic starting points are: four-dimensionally
We are in the beginnings of the water man age, in which four-dimensional the way of life and thinking outweigh. In the course of this age we will learn holistic to live. All diseased, degenerate forms are back developed by the law of the holistic viewpoint into the healthy form. This Holistic in the water man age means lived courageous acting LOVE.
Dark field blood diagnostics
Method of Professor Dr. Guenther Enderlein (1872-1968), that primarily a biologist and a zoologist was 1916 came from Enderlein a first report over a revolutionary reorganization of the bacteriology.
Dr. William of Brehmer (1883 - 1958) discovered 1928 the blood parasites Siphonosphora polymorpha in the red blood corpuscle of humans, which can develop itself further under certain conditions to diseased forms. The special at of Brehmer the method is coloring native or vital blood on a slide, whereby certain high valence forms become visible. By the advancement of the technology to the phase contrast microscope, it is to be regarded us today possible certain forms without coloring immediately.
Most important aspect also for of Brehmer is clarifying the acid Base environment in the organism. It developed for it the Haemo Ionometer. Robert-Koch-Institute with the Humboldt university in Berlin, under which line of the then world-famous Hematology Professor Dr. Victor Schilling confirmed to 1935 that Siphonosphora polymorpha the second genuine blood parasite is, which develops in the Erythrocyte.
First up to then admitted blood parasite was the Plasmodium malaria. Thus Brehmers discovery was scientifically certified and in the medical professional world recognition. The exciters go through a specific cycle, as the training medicine and bacteriology accept it with malaria as natural. The training medicine until today recognizes the development stages of viruses, bacteria and mushroom forms however not on. Although there is nevertheless no exception of the law of the eternal change and the unit of the macrocosm with the microcosmic (e.g. Qualquappe' Frog, Raupe' Butterfly) in whole nature.
Cyclogenie means the transformation and migration of all pathogen and not pathogen germs by all phases (valences) of the border of the visibility, and among them the virus range, over the higher valence phases of the text book-in accordance with-eaten Kokken and the staebchen up to the kulminanten phases of the mushrooms and their Myzelien.
The bacteria core (Mych) plays an important role, the moreover the pH value, i.e. the acid Base household of the organism of humans (to the comparison: as is the case for the aquarium). Only if the environment is not correct, the pathogen development can take place. Either asexual by division or on sexual way by Sprouting after preceding nuclear fusion. The principle of the Polymorphic was confirmed 40 years after Enderlein by the Nobel leather castle.
more information:
http://www.dreddyclinic.com/faq_live_blood_microscopy_1.htm
Sunday, February 24, 2008
Death By Vaccine
Dr. Young has stated that the use of vaccinations, antibiotics and antifungals will only poison the body leading to the one sickness and one disease - latent tissue acidosis and then death.
All vaccinations, antibiotics and antifungals are the acids of morbid fermentation of plant, animal and human matter and when ingested or injected, it only proves that you can poison the body and then hopefully live through it.
The day will soon come when scientists will proclaim that the use of vaccinations, antibiotics and antifungals were and are harmful to the human body and should not be used under ANY circumstances.
In the words of Thomas Edison, 'The Doctor of the Future will give no medicine, but will involve the patient in the proper use of food, fresh air, and exercise.'
The future that Thomas Edison speaks is here and now! Read on to understand and to see for yourself the course we have been walking for the last several centuries and how things must change before it is to late.
1798 General vaccine programs against cowpox instituted in the US.
1801 First widespread experimentation with vaccines begins.
1802 The British government gives Edward Jenner £10,000 for continued
experimentation with 'smallpox vaccine.' The paradigm that vaccines
provide 'lifetime immunity' is abandoned, and the concept of 'revaccination' is
sanctioned.
1822 The British government advances Edward Jenner another £20,000 for
'smallpox vaccine' experimentation. Jenner suppresses reports which
indicate his concept is causing more death than saving lives.
1844 Fredrich Loeffler isolated the diphtheria bacillus from the throats of patients.
1881 Sternberg in his own lab isolated the pneumococcus
1882 Robert Koch isolates the tubercle bacillus
1883 Robert Koch isolates the cholera bacillus.
1883 Max Von Pettenkofer suggested that Koch's bacteria were only one of the many factors in the causation of cholera. He prepared test tubes thick with lethal cholera bacteria and he and several of his students drank them down with no side affects.
1888 Bacteriological Institute opens in Paris for experimentation with animals and production of vaccines and sera. Other institutes open around the world modeled after the Paris Institute.
1888 Bacteriological Institute in Odessa, Russia tries its hand at a vaccine for anthrax. Over 4500 sheep are vaccinated; 3,700 of them die from the vaccination.
1909 New York Press, January 26, 1909 publishes a report by W.B. Clark which states, 'cancer was practically unknown until cowpox vaccination began to be introduced. I have seen 200 cases of cancer, and I never saw a case of cancer in an unvaccinated person.' Scientific evidence begins to mount that where human lymph is employed in a vaccine, syphilis, leprosy and TB soon follow. Where calf lymph is employed in the creation of a vaccine, TB and cancer soon follow. (Cancer and Vaccination by Esculapius).
1911 The head of French Public Health for the French Army said that germs alone were 'powerless to create an epidemic.'
1912 First whooping cough (Pertussis) vaccine created by two French bacteriologists, Jules Bordet and Octave Gengou, who wanted to use it in Tunisia. After they grew Pertussis bacteria in large pots, they killed it with heat, mixed it with formaldehyde (used to embalm bodies) and injected it into children.
'Vaccinations, Not a Virus, Is Responsible for Spanish Flu - 1918'
Dr. Robert O. Young
1933 a British science team to identify the first filterable bacteria in man, yet propaganda says that the virus of Spanish flu killed millions of civilians and soldiers during the pandemic from 1918 to 1920.
Many would have us believe that all those American soldiers who died from non-combatant causes died from Spanish flu. However, U.S. Army records show that seven men died after being vaccinated.
A report from U.S. Secretary of War Henry L Stimson, the deaths were not only verified but also there had been 63 deaths and 28,585 cases of hepatitis reported as a direct result of yellow fever vaccination during only six months of the war. Plus, the yellow fever vaccination was only one of the 14 to 25 shots given to recruits.
1911 vaccinations became a requirement in the U.S. Army. Cases of typhoid and vaccinal diseases increased rapidly, according to Army records.
1917 The death rate from typhoid reached the highest point in the history of the U.S. Army after America entered the war.
In 1917, 19,608 men were admitted into army hospitals due to antityphoid inoculation and vaccinia, according to a report of the Surgeon-General of the U.S. Army; and this doesn't take into account others whose symptoms were attributed to other causes.
The army doctors knew all these cases of disease and death were due to vaccination and were honest enough to admit it in their medical reports. Army doctors tried to suppress the symptoms of typhoid with a stronger vaccine, however it caused a worse form of typhoid, paratyphoid. They then concocted an even stronger vaccine to suppress the previous one and created an even worse disease--Spanish flu.
After the war, this was one of the vaccines used to protect a panic-stricken world from the soldiers returning from WWI battle fronts infected with dangerous diseases.
The rest is history.
1918 Great influenza epidemic attributed to widespread use of vaccines that killed up to 100 million people.
1921 BCG tuberculosis vaccine developed.
1922 A study by Samuel Torrey Orton connects emotional disturbance with neurological problems. This insight was lost after World War II when psychology, psychiatry and psychoanalysis became popular, breaking the connection. The emotional disturbances caused by vaccines then became financial fodder for the new psych-industries. With the causes suppressed, a new industry was born.
1925 Danish researcher Thorvald Madsen tries a modified Pertussis vaccine during an epidemic in the Faroc Islands. It did not prevent Pertussis. (See 1933).
1925 General vaccine programs against tuberculosis began in the United States.
1927 British government appoints a committee to inquire into 'vaccine lymph', as it is noticed that the 'glycerinated calf lymph' used in vaccinations causes deaths from 'sleepy sickness'. Two London professors bring notice of the problem to the government in 1922. It takes 5 years before the government responds.
1930 Max Theiler develops a yellow fever vaccine.
1931 Roosevelt endorses polio 'immune serum', precursor to vaccines in 1950's.
1932 Diptheria vaccines injure 171 and kill 1 in Charolles, France.
1933 Danish researcher Thorvald Madsen discovers the Pertussis vaccines ability to kill infants without warning (SID). He reports that two babies vaccinated immediately after birth died in a few minutes.
1933 American researchers report that children react to Pertussis vaccine with fever, convulsions and collapse.
1936 Pertussis vaccine introduced in the United States. Autism begins to appear in children shortly thereafter.
1936 Diptheria vaccine injures 75 in France.
1943 American vaccine researcher Pearl Kendrick reports that adding a metallic salt seemed to heighten the capacity of the Pertussis vaccine to produce anti-bodies. (Metal salt is an 'adjuvant' in this way). Some metallic salts used are those of aluminum (alum). Pearl Kendrick is the researcher that urged that Pertussis vaccine be combined with Diptheria vaccine. Later the Tetanus vaccine was added, producing the nefarious DPT Vaccine.
1943 General vaccine program against influenza begins in the US.
1944 Health Practitioners Journal, June 1944, reports Dr. S.S. Goldwater, the New York Commissioner of Hospitals states 'as a result of the drugs, vaccines and other suppressive treatments used to check diseases, chronic diseases are growing at such a rate that America may become a nation of invalids.'
1945 Japan surrenders twice, followed by US bombing of Hiroshima/Nagasaki and a third and final surrender. The Allies mandate compulsory vaccination in Japan. The first cases of autism follow pertussis vaccine introduction.
1946 US Government Pertussis vaccine expert Margaret Pittman and FDA's Charles Kendrick decide to test Pertussis vaccine by injecting it into the brains of mice and see how many survive.
1946 Werne and Garrow describe the deaths of identical twins within 24 hours of their second Pertussis shot.
1947 Matthew Brody at the Brooklyn Hospital gives detailed descriptions of two cases of brain damage leading to death in children receiving Pertussis shots.
1947 Charles Posner of the Harvard Medical School Department of Neurology writes, 'almost any vaccination can lead to noninfectious inflammatory reaction involving the nervous system. The common denominator consists of vasculopathy that is often associated with demyelination.' (demyelination is the stripping of the insulation away from the nerves).
1947 The British Medical Research Council begins testing 50,000 children in Britain with the Pertussis vaccine. All children tested are more than 14 months old (not newborns). Eight infants had convulsions within 72 hours of the shot, 34 had convulsions within 28 days of the shot. British doctors denied a connection between the vaccine and the convulsions, declaring the tests a success and began administering it to all British children.
Despite the fact that none of the tests were conducted on children under 14 months old (newborns & babies), the United States holds the tests in evidence that the vaccine is safe for newborns as young as 6 weeks of age. The testing would continue until 1957.
1948 Randolph K. Byers and Frederick C. Moll of the Harvard Medical School publish an article describing children who had suffered brain damage after receiving Pertussis vaccine. The findings provided the first clear evidence that the vaccine caused the serious neurological complications in children.
1948 Randolph Byes and Frederick Moll of Harvard Medical School validate that severe neurological disorders follow the administration of DPT vaccine. The research was performed at Children's Hospital in Boston and published in Pediatrics magazine. Nothing was done by physicians to halt the use of DPT vaccine.
1948 A study on Pertussis vaccine reaction is done by Randolph K. Byers and Frederick C. Moll of the Harvard Medical School. They examine 15 children who had reacted violently within 72 hours of a Pertussis vaccination. All the children were normal before the shot. None had ever had a convulsion before. One of the children became blind, deaf, spastic and helpless after being given the Pertussis shot. Out of the 15 children, 2 died and 9 suffered from damage to their nervous system. Physicians were displeased by these results.
1948 England bans smallpox vaccine.
1948 North Carolina polio cases number 2,498. See 1949.
1948 Louis Sauer makes an interesting observation at an AMA meeting where Pertussis vaccination was discussed. Louis Sauer points out that 'the neurological damage caused by Pertussis vaccine is the same as the damage caused by Pertussis (whooping cough -- Which is logical, because they use the bacteria in the vaccine). According to Sauer, 'a customary prophylactic dose of Pertussis vaccine seems to illicit a chain of nervous system reactions and in some cases irreversible pathological changes in the brain. These findings resemble those encountered in cases of severe whooping cough (Pertussis).' In other words, the vaccine is causing the disease condition.
1949 US Public Health Service Division of Biologics Standards establish a national potency test for Pertussis vaccine, and modify it in 1953 to establish potency limits. Despite this, the Pertussis vaccine that is pronounced 'safe' still causes minimal brain damage (MBD) in humans.
1951 Theiler wins Nobel for work on yellow fever vaccine.
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).
1953 At the University of Zurich, Dr. S.Kong of the Pediatric Clinic compiles a list of 82 cases of Pertussis vaccine damage from world literature.
1953 The Swedish conduct a study on the Pertussis vaccine. Anna L. Annell, a Swedish researcher, writes a major work on Pertussis which indicates that 'pertussis vaccine may be associated with the most varying kinds of cerebral complications which may be cortical, subcortical or peripheral.'
Encephalitis after vaccination is known to produce the same range of disabilities and impairment. Annel also wrote, 'during the past few decades certain of the epidemic children's disease, measles in particular, have shown an increased tendency to attack the central nervous system. After the 1920's a large number of cases involving CNS damage were reported.
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.
1954 A study on 'neurologic sequelae of prophylactic innoculation' summarized state-of-the-art knowledge in noting that the common factor in the pathologyof encephalitis from vaccination is 'anaphlactic hypersensitivity'.
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.'
1955 Measles death rate has naturally declined, without vaccines, to .03 per 100,000 by 1955.
1955 At the University of Illinois School of Medicine, Department of Neurology, Niels Low shows that the EEG of infants is sometimes altered by a DPT shot,concluding that significant cerebral reactions and neurological changes occur.
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.
1955 Despite the sky rocketing cases of vaccine-induced polio, the AMA, NFIP and USPHS claim a reduction of 40-50%.
1955 Idaho brings its Salk vaccination program to a halt on July 1, 1955.
Utah does the same on July 12, 1955.
1955 Boston Herald newspaper reports on April 18, 1955, features an article entitled 'Drug Companies Expecting Big Profit on Salk Vaccine', which stated. 'A spokesman for Parke-Davis, which made 50% of the Salk vaccine, said 'now that it has been declared safe, we can get back the millions we invested in the development of the Salk vaccine and make a profit out of it. Our company will made over $10 million on Salk vaccine in 1955.'
1955 Rhodes and Company, Wall Street brokers specializing in drug securities, estimate that the gross revenue of the six vaccine houses licensed to produce and sell Salk vaccine would be about $60 million, with profits of $20 million.
1955 The CIA conducts a biological warfare experiment in the Tampa Bay area in Florida with agents withdrawn from an Army CBW center. A sharp rise in whooping cough (Pertussis) cases occurs, including 12 deaths, following the test.
1955 Washington Bureau of the Detroit Free Press reports, on June 3, 1955, that 'The USPHS reported that more children who received Salk shots made by the Wyeth Labs suffered polio more than could normally be expected;'
1955 AMA Conference in Atlantic City, New Jersey. Article by James C. Spaulding who covered the conference was published in the AMA Journal, June 19,
1955, 'A policy of secrecy and deception has been followed by the National Foundation for Infantile Paralysis and the US Public Health Service in the polio vaccine programs. The nation's physicians were prevented from learning vital information about the trouble with Salk vaccine. The US Public Health Service had an advisory group made up almost entirely of scientists who were receiving money from the National Foundation of Infantile Paralysis, which was exerting pressure to go ahead with the program even after Salk vaccine was found to be dangerous.' Spaulding further said, 'the Infantile Paralysis Foundation kept secret the fact that live virus was detected in four out of six supposedly 'finished and safe' lots of vaccine.'
1955 Salk Polio Vaccine again used in the US. Cases of polio skyrocket again in the United States.
1955 Reported that doctors on the staff of the National Institutes for Health are avoiding vaccination of their children with the Salk vaccine, and that after experimenting with 1200 monkeys, they declared the Salk vaccine worthless as a preventative and a danger to take.
1955 First vaccinated generation become adolescents.
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 Dr. Graham W. Wilson, director of Britain's Public Health Laboratory Service, who knew about the NIH Salk vaccine trials, says 'I do not see how any vaccine prepared by Salk's method can be guaranteed safe.'
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.
1955 Surgeon General Scheele (who never practiced medicine a day in his life!) goes on public radio saying 'I have complete confidence in the Salk vaccine. I urge doctors to continue vaccinations.'
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 Governor Knight of California asks the legislature for $3 million in order to insure vaccination for all those under 40 years old with Salk polio vaccine. The newspapers report that corporate profits from the Salk vaccine will be in excess of $5 billion. (Feb 6, 1957). Governor Knight notes there are 4 million Californians under 40 and signs the bill.
1957 Pertussis vaccination programs exist in all industrialized nations, with the US leading the way. The vaccine is promoted as 'risk free'.
1957 Scientists isolate a series of Simian (monkey) viruses and discover that these same viruses contaminate polio vaccines. SV-40 found in both Sabin and Salk polio vaccines. (made since early '50s), Information not made public. The same vaccines continued to be used until the early 1960's.
1958 World literature now contains 107 cases of severe reaction to Pertussis vaccine (93 of those cases were in the US). At the Fountain Hospital in London, Dr. J.M. Berg analyzed the 107 cases and found that 31 of them showed signs of permanent brain damage. Berg calls attention to the danger of mental retardation as an effect of the Pertussis vaccine and emphasizes that 'any suggestion of a neurological reaction to a Pertussis vaccination should be an absolute contraindication to further inoculation.' The United States medical establishment ignores and suppresses the data. American physicians maintain that the damage caused is small compared to 'lack of 'serious' reactions in children vaccinated.' No data has ever been found to justify a basis for this conclusion.
1958 Verdict of $147,000 rendered against Cutter Laboratories in California for the crippling of two children with the Salk polio vaccine. Cutter Labs was the only vaccine manufacturer not part of the Rockefeller Trust.
1959 The United States never conducts its own clinical trials on Pertussis vaccine, but instead relies (as it still does today) on data collected by Britain's Medical Research Council in clinical trials in England in the 1950's for 'proof of vaccine safety and effectiveness in newborns and children.' Interestingly, Britain's trials on 50,000 British children were performed on children more than 14 months old. None of the children were newborns.
1959 National Institutes of Health (NIH) approves licensing of Quadrigen vaccine for children, containing Pertussis, Diptheria, Tetanus and Polio vaccines. The new combination vaccine was found to be highly reactive and was withdrawn from the market in 1968 after parents started filing lawsuits against Parke- Davis for vaccine damaged children.
1959 Pertussis vaccine found to have allergenic effect on animals.
1960 British Medical Journal publishes an article by Swedish vaccine researcher Justus Strom, who stated that the neurological complications from the disease Pertussis are less than that in the Pertussis vaccine. Strom also pointed out that 'whooping cough (Pertussis) had changed and had become a milder disease, making it questionable whether universal vaccination against it is justified.'
1960 General vaccination program for measles begins in the United States.
1960 It is estimated in 1960 that over 1,000,000 children have vaccine-caused disabilities, including learning difficulties and school behavioral problems, behavioral disturbances, allergies, speech difficulties, visual problems, and problems in adjustment and coping.
1961 A senior school medical officer in Northern England, J.M. Hooper, finds that parents are beginning to refuse to bring children for a Pertussis booster shot, based on earlier violent reaction to the 'vaccination.' Children were suffering from collapse, vomiting, and uncontrollable screaming. No one paid attention to these warnings.
1961 Sabin polio vaccine immunization campaign.
1963 American researcher John F. Enders creates a measles vaccine. Mass inoculations begin.
1963 Children vaccinated with killed measles vaccine between 1963 and 1967 develop Atypical Measles Syndrome (AMS). Studies suggest the children's reshponse to the 'wild' measles virus is 'altered' and that the severity and persistence of symptoms suggests encephalopathy (brain damage.) See 1967.
1964 Reward of $30,000 offered to prove polio vaccine was not fraud. No takers.
1965 US Government's leading Pertussis vaccine specialist, Margaret Pittman, (until 1971) states, 'Bordetella Pertussis is unique among infectious bacteria in its marked ability to modify biological processes.'
1965 Congress passes the Immunization Assistance Act. More states made their vaccination programs mandatory/obligatory.
1967 The FDA stops the use of an experimental cancer vaccine which was producing significant results. Developed by James Rand and Eernest Ayre, a recognized cancer specialist. The Rand vaccine produced significant improvement in terminal patients in over 30% of patients. It cured tumors and breast cancer in four to six months, without radiation, surgery or chemotherapy. The FDA Commissioner was James L. Goddard, the same man who persecuted the use of DMSO. Goddard used the DMSO issue in 1966 in an attempt to foster a medical dictatorship in the US in collusion with the medical and pharmaceutical industries, and remove viable treatments from public access.
1967 At the Bland-Sutton Institute of Middlesex Hospital in London, George Dick writes, 'it has been long known that increasing the number of Pertussis bacteria per dose of vaccine increases the frequency of reactions. It would be surprising if decreasing the size of the infants receiving a particular vaccine did not also increase the reactions.' A violation of a standard axiom in medicine, which matches the size and weight to an amount of substance. (Why are newborns getting the same dosage as an adult?).
1967 Dr. Vicent Fulginiti, M.D., former chairman of the American Academy of Pediatrics Committee on Infectious Diseases, asserts that inactivated measles vaccine should no longer be administered. See 1963.
1967 Killed measles vaccine is discontinued in the United States.
1967 General vaccination program for Mumps begins in the United States.
1967 Science magazine (10/20/67) features article on Joshua Lederberg of the Department of Genetics, Stanford University School of Medicine. Lederberg notifies the scientific world that 'live viruses (as in vaccines) are genetic messages used for the purpose of programming human cells' and 'we already practice biological engineering on a rather large scale by use of live viruses in mass immunization campaigns'
1970 Due to the increasingly mild nature of whooping cough (Pertussis), infant deaths cease from naturally acquired Pertussis in Sweden. Deaths associated with vaccine continue. Sweden stops Pertussis vaccination in 1970.
1970 A study by Pittman reveals Pertussis vaccine can induce hypoglycemia due to increased production of insulin. (Ref: DPT shots). Study is corroborated in 1978 by Hannick and Cohen and by Hennessen and Quast in West Germany. Result: Pertussis and DPT vaccines can cause diabetes.
1972 British Journal of Psychiatry #120 reveals that 'psychotic disorders may be caused by viral infections.' (Ref: viruses induced by vaccines).
1973 The field of genetic engineering is opened by advances in scientific research, making way for creation of recombinent micro-organisms and new viral structures in the laboratory. The U.S. military applies the technology to its chemical and biological weapons program, claiming overtly that such work is 'to develop defensive vaccines'.
1974 British researcher George Disk estimates that there are 80 cases of severe neurological complications from Pertussis vaccine annually. Over 33% of these children died and another 33% were left with brain damage. Dick maintains he is not convinced that the community benefit from the vaccine outweighs the damage.
1974 The Association of Parents of Vaccine Damaged Children is formed in Britain, & pressures the government to study adverse reactions to Pertussis vaccine.
1975 Federal Drug Administration Bureau of Biologics concludes that Diptheria toxoid (vaccine) is 'not as effective an immunizing agent as might be anticipated.' They admit that Diptheria may occur in vaccinated people, and note that 'the permanence of immunity induced by the toxoid is open to question.'
1975 Japan stops using Pertussis vaccine following publicity about vaccine-related deaths.
1976 FDA Pertussis vaccine specialist Charles Manclark comments 'Pertussis vaccine is one of the most troublesome products to produce and assay. It has one of the highest failure rates of all products submitted to the Bureau of Biologics for testing and release. Approximately 15-20% of all lots which pass manufacturer tests fail to pass the tests of the Bureau.'
1976 According to a letter from the British Association for Parents of Vaccine Damaged Children, published in the British Medical Journal of February 1976, 'two years ago we started to collect details from parents of serious reactions suffered by their children to immunizations of all kinds. In 65% of the cases referred to us, reactions followed 'triple' vaccinations. The children in this group total 182 to date. All are severely brain damaged, some are paralyzed, and 5 have died during the past 18 months. Approximately 60% of reactions (major convulsions, collapse, screaming) happened within 3 days and all within 12 days.
1976 Dr. Jonas Salk, creator of the polio vaccine, says that analysis indicates that the live virus vaccine in use since the 1960's is the principle, if not sole cause of all polio cases since 1961.
1976 More than 500 people receiving flu vaccinations become paralyzed with Guilain-Barre Syndrome.
1977 A Blue Ribbon Panel is convened to investigate the reason for the drop in the general IQ of the United States. Seventy-nine theories were advanced, but none of them satisfactorily explained the drop in mental capacity of the US population. The idea that vaccines could be part of the problem was not brought up. Y.L. Warten, 1977. (The Prussian education system is also part of the problem, for those volkschuelen).
1977 The British government is pressured by the publicity following the new data about Pertussis and DPT vaccinations.
1977 The University of Glasgow in Scotland, Department of Community Medicine, Dr. Gordon Stuart, publishes a study analyzing 160 cases of adverse reaction and neurotoxicity following DPT vaccination. In 65 of those cases, reactions to DPT shots included convulsions, hyperactivity and severe mental defect. In a stern statement, Stuart says, 'it seems likely that most adverse reactions are unreported and/or overlooked.'
1977 The British government conducts the National Childhood Encephalopathy Study (NCES) which tests the connection between vaccinations and neurological disease.
1977 (Mar) Jonas and Darrell Salk warn live virus vaccines produce same disease.
1978 According to Charlotte Parker of the University of Texas Department of Microbiology, the nature of the organism Bordetella Pertussis means that different lots of vaccine made from the same strains sometimes show different properties.
1978 In the United States, the FDA finances and conducts a study at UCLA from January 1, 1978 to December 15, 1979 called 'Pertussis Vaccine Project: Rates, Nature and Etiology of Adverse Reactions Associated with DPT Vaccine'. The results of the study were published in Pediatrics in November.
1978 In England, Griffith studies pertussis vaccine reactions in children, noting a case in which a boy experiences brain damage 3 days after vaccination and dies 27 days later due to injection of triple vaccine.
1981 The unpublished contractors 'Final Report' was submitted to the FDA on March 18, 1980 (a year earlier) and contained revealing data. The study found a higher incidence of adverse reactions to the DPT shot than any previously reported in literature. After the study had run nine months, the FDA convened a Pertussis Symposium, at which it was revealed that 'the most striking finding in this preliminary analysis is the high frequency of persistent crying, episodes of convulsions and collapse following DPT immunization.' Because of these findings, the study was curtailed from the planned examination of 50,000 vaccinations to only 17,000. The UCLA FDA study also found that systemic reactions in the central nervous system were present in 50% of the vaccinations. Because of this potentially damaging information, the FDA placed an arbitrary time limit of 48 hours within which reactions had to occur, despite ongoing data which indicates that serious reactions occur after that time
limit, in order to limit the statistical data and conceal the extent of the problem from the population. (See 1981).
In 1988, an FDA-sponsored follow-up study of the '18' children with neurological reactions concluded 'no significant neurological impairment.'
A 1988 re-examination of those same children by an independent researcher, pediatric neurologist Ronald Gabriel, not associated with the FDA, proved that the FDA lied--only 4 of the 18 were normal. The results were presented at a May 1980 meeting of the Institute of Medicine. Results indicate that encephalopathy is followed by subtle learning, behavioral and neurological problems. (Note: See the book Vaccination, Social Violence and Criminality: the Medical Assault on the American Brain, by Harris Coulter,1990. The FDA is continuously involved in criminal conspiracy and racketeering along with pharmaceutical and chemical companies in the United States.)
1978 Trials of Hepatitis B vaccine in New York City on non-monogamous males between 20 and 40 years old. Homosexuals receive a different vaccine.
1979 Two pediatricians in California report brain swelling associated with DPT vaccine administration.
1979 New rubella vaccine introduced. See 1988.
1979 The US Food and Drug Administration (FDA) funds a study which represents the first significant 'attempt' to evaluate reactions to the DPT shot. The study is conducted at the University of California (UCLA) and was published in Pediatrics in
1981. After studying 16,000 DPT and DT vaccination cases, they concluded that the Pertussis (P) element of the DPT shot was the element causing reactions. They also found that the incidence of all DPT reactions was much higher in the population than had been suspected or reported in the scientific literature. Despite these results, even in 1994 physicians promote Pertussis vaccine with confidence, pay little attention to identification of high risk children, and do not carefully observe contraindications. Parents are legally required to vaccinate their children with Pertussis before entering them in school. (See 1982)
1980 Estimated 2 million American children with vaccine-caused disabilities.
1981 At the headquarters of the Occupational Safety and Health Administration (OSHA), the director of the OSHA office of carcinogenic identification, Dr. Peter Infante, pointed out that a Current Intelligence Bulletin (CIB) on formaldehyde was 'an important document assessing formaldehyde's cancer causing potential'. The top bureaucracy at OSHA were embarrassed at the release of the truth, and tried to dismiss Infante. On July 27th, Infante writes Dr. John Higginson, director of the International Agency for Research on Cancer (IARC), disagreeing with the IARC decision to conceal the carcinogenic nature of the substance. Formaldehyde is a common component of vaccines.
1981 Britain conducts the National Childhood Encephalopathy Study, and finds that there exists a significant correlation between serious neurological illness and Pertussis vaccination occurring within 7 days of the shot. In the US, the FDA limits statistical data to 48 hours in order to conceal damaging data and eliminate data on deaths and damage occurring after that period of time.
1981 Japan begins use of a new childhood Pertussis vaccine, recommended to be given as 4th and 5th dose. US vaccine used for 1st,2nd,3rd doses. 1981 In Britain, Dr. D.L. Miller reports to the NCES on an analysis of the first 1,000 cases of neurological illness. He reported 'a significant association was shown between serious neurological illness and Pertussis (also DPT) vaccine.'
1981 New England Journal of Medicine (11/26/81) publishes a study showing that tetanus vaccines cause T-cell ratios to drop below normal, with the greatest decrease after two weeks. The altered ratios were found to be similar to those found in AIDS victims.
1982 A reporter at WRC-TV in Washington, DC breaks a story on Pertussis vaccine reactions in the documentary 'DPT: Vaccine Roulette', which generally informs the American public that their children are at risk from Pertussis vaccinations. (See 1988)
1982 Homosexuals in Chicago, St. Louis, Denver, Los Angeles and San Francisco get Hepatitis B vaccine.
1983 Bellman, Ross and Miller publish a study of 269 cases of infantile spasms which returns to the establishment position that 'DPT vaccines do not cause infantile spasms, but may trigger their onset in those children in whom the disorder is 'destined to develop'. (Note: Using this logic, if one can)
1983 Stanford University Study on Pertussis Vaccine. Lawrence Steinman and colleagues at Stanford University School of Medicine perform a study which reveals that children with allergies may overreact to Pertussis vaccine.
1984 - The 1984 Connaught Laboratory package insert for DPT vaccine cites a 1978 Scandinavian study linking the vaccine to the development of hemolytic anemia and warns that this is a contraindication. By 1991, they would remove this warning from their package inserts in order to conceal this data. This kind of anemia is typified by weakness and periodic loss of consciousness.
1984 A complaint was filed by a group of US physicians with the UN Center for Human Rights in Geneva, entitled 'A Complaint Against Medical Tyranny As Practiced in the United States of America: American Medical Genocide'; the existence of the report was suppressed by the Bush Administration and the media. Reprinted in The Leading Edge in Oct/Nov 1994.
1984 Shaywitz Study at Yale Medical School Pediatrics revealed that 'minimal brain damage is perhaps the most common and time-consuming problem in current pediatric practice.'
1984 Wyeth Laboratories package insert for DPT vaccine states, 'The occurrence of Sudden Infant Death Syndrome (SIDS) has been reported following administration of DTP vaccine' and that 'approximately 85% of SIDS cases occur in the period 1 through 6 months of age, with the peak incidence at age 2 to 4 months.'
Two years later in 1986, the Wyeth insert stated, 'SIDS has occurred in infants following administration of DPT' but went on to state that 'one study showed that there was no causal connection'. (Note: One wonders who paid for and did that specific study.)
1984 CDC acknowledges that 60% of those receiving hepatitis vaccine are HIV +.
1985 Tests developed to detect simian viruses in vaccines.
1985 The Assistant Secretary of Health, Edward Brandt, Jr., M.D, testifies before a Senate Committee, 'every year 35,000 children suffer neurological complications because of DPT vaccine.' (May 3, 1985).
1985 Hemophilus Influenza type B (HIB) vaccine approved for general use in US. The HIB vaccine is often referred to as the 'meningitis' vaccine, but meningitis has several causes.
1986 150 lawsuits pending against DPT vaccine makers.
1986 National Childhood Vaccine Injury Act. Administered by the US Claims Court in Washington, DC, which does recognize an association between the DPT shot and infantile spasms. The court awarded $2 million to a body in 1989 relative to a reaction to DPT vaccine.
1986 National Health Survey finds that between 1969 and 1981, the prevalence of 'activity-limiting chronic conditions' in children increased by 44%, from 2.9 million children to 3.8 million children. Almost all of the increase happened between 1969 and 1975. Most of these conditions are readily associated with post-encephalitic syndrome. Childhood respiratory disease during this period increased 47%, childhood asthma increased 65% (with deaths from asthma increasing), mental and nervous system disorders increased 80%, personality and other non-psychotic disorders (behavior disorders, drug abuse and hyperactivity) increased 300%, diseases of the eyes and ears (especially otitis media) rose 120%, and cases of hearing loss in the ears rose 129%. All of these increases were identical in both high and low income groups. For the same period of time, levels of disease not associated with vaccine damage remained unchanged.
1986 Connaught Laboratory, manufacturer of DPT vaccine, changes the product info sheet to warn against 'allergies' and 'anaphylactic sensitivity'.
1986 Connaught Laboratories package insert for their DPT vaccine reads 'some data suggests that fever is more likely to happen in those who have had local reactions, and that local reactions are more likely to occur with increasing numbers of doses of DPT.'
1987 Centers for Disease Control (CDC) releases a study indicating that the Hib vaccine shows an efficacy (effectiveness) rate of 41%. Children were found to be 5 times more likely to contract the disease than those not vaccinated.
1987 66 Japanese victims of Pertussis vaccine receive huge damage awards from the Japanese government.
1988 Lederle Laboratories package insert for DPT vaccine reads 'Pertussis vaccine has been associated with a greater proportion of adverse reactions than many other childhood vaccinations. Local reactions are common after administration of DTP, occurring in 35-50% of recipients. Febrile [feverish] reactions are more likely to occur in those who have experienced such responses after prior doses.'
1988 Two scientific studies find that new rubella vaccine introduced in 1979 was found to be the cause of Chronic Fatigue Syndrome (Epstein-Barr virus), an immune disorder first reported in 1982.
1988 Robert S. Mendelsohn M.D, publishes material indicating that Dr. John Seal of the National Institute of Allergy and Infectious Disease believes that 'any and all flu vaccines are capable of causing Guillain-Barre.'
1988 New 'conjugated' [joined together] HIB vaccine approved for use in children at least 18 months old in the United States. HIB = Hemophilus Influenza Type B.
1990 Health Consciousness magazine features article entitled 'Live Virus Vaccines and Genetic Mutation' by H.E.Buttram, M.D, in which it is determined that 'the physical invasion of the human body by foreign genetic material may have the immediate effect of permanently weakening the immune system, setting in motion a new era of autoimmune diseases.'
1990 The US Public Health Service Immunization Practices Advisory Committee (ACIP) and the American Academy of Pediatrics considers high-pitched screaming after a Pertussis (DPT) vaccination an absolute contraindication to further Pertussis vaccine.
1990 Pediatric neurologist Dr. John H. Menkes, professor emeritus at UCLA, reports on 46 children experiencing neurological adverse reaction within 72 hours of a DPT shot. Over 87% of the children reacted with a seizure, 2 children died and most surviving children became retarded, with 72% having uncontrollable seizure disorders. Menkes conclude, 'Pertussis vaccine encephalopathy (brain damage) is not a myth but rather a serious complication of immunization.'
1990 U.S. Claims Court, as of October 31, 1990, indicates that 'several thousand claims for compensation from injuries or death caused by vaccines have already been filed.' National Vaccine Information Center.
1990 Estimated 3 million in US with vaccine-caused disabilities.
1990 In December of 1990, a federal regulation was adopted permitting the FDA to circumvent US and International laws forbidding medical experimentation on unwilling subjects. This regulation permits the FDA to inject American military with unapproved experimental drugs or vaccines without informed consent. The FDA merely needs to deem it 'not feasible' to obtain the soldiers permission. See Health Letter, Washington, DC. Public Citizens Health Research Group '400,000 Human Guinea Pigs in the Persian Gulf', Feb 12, 1991. See 1991 Gulf War Entry.
1991 Operation Desert Storm. Bush stops war after 100 hours at preserve Iraq as a threat. American troops are given experimental vaccines against biological agents. Within months thousands of troops sicken with the acids that cause cancer. Disease deemed 'Gulf War Syndrome'. Government denies responsibility. Over 8,000 troops were vaccinated with Botulism, over 150,000 troops were given anthrax vaccine, and all 500,000 troops were given Pyristigimine, an experimental nerve agent. All drugs were experimental.
1991 New York Times, Mar 17th, 1991 'US Vaccine Plan Uses Welfare Offices' indicates the Federal government has considered denying welfare and nutritional benefits to families who refuse vaccinations.
1991 The US Public Health Service Advisory Committee on Immunization Practices (ACIP) drafts new guidelines which eliminate most contraindications to Pertussis vaccine. Essentially, this results in a denial or cover-up of most reactions on the grounds that 'there is no proof the vaccine causes brain ' They base their position on several studies financed by vaccine manufacturers conducted in the late 1980's by vaccine policymakers such as Dr. James Cherry and Dr. Edward Mortimer, who sit on the ACIP Committee and are also paid consultants to US Pertussis vaccine manufacturers, resulting in biased and flawed studies in order to prove 'no cause and effect' between the Pertussis vaccine and permanent brain damage. US vaccine policymakers are the CDC and the American Academy of Pediatrics. All this, despite decades of experience indicating the opposite conclusion. (Note: This policy constitutes criminal neglect, racketeering and conspiracy!).
1991 The 'conjugated' HIB vaccine introduced in 1988 is extended for use in infants as young as two months. It becomes mandated in 44 states in the US.
--The Olympian, Nov 23, 1994. Pertussis also can cause Sudden Infant Death.
1991 The CDC begins the process of mandating Hepatitis B vaccinations for all infants in the United States. Many infants receive multiple doses from birth.
1992 Lancet, Journal of the British Medical Association, reports (3/7/92) that the oral polio vaccine used in the mid 1970's to treat recurrent herpes was contaminated with a number of potentially dangerous retroviruses, and may have seeded HIV among Americans'.
1992 Article in the Washington Post, Nov 2, 'On Vaccinating Safely' and Dec 14th press release by the National Vaccine Information Center indicate release by the FDA of a report acknowledging more than 17,000 adverse events-- including more than 350 deaths--following vaccination, all in a 20 month period ending July 31,
1992. Reported events number far less than actual events, so number is actually larger, perhaps 170,000 or more. 1992 From 1988 to 1992, over $249 million has already been awarded due to hundreds of deaths and injuries caused by mandated vaccines. Thousands of cases are still pending. The permanent injuries from vaccines include, but are not limited to, learning disabilities, seizure disorders, mental retardation, and paralysis. Many of the awards for pertussis vaccine deaths were initially (and wrongfully) misclassified as Sudden Death Syndrome (SIDS).
1992 Centers for Disease Control (CDC) reports that 87% of all cases of polio in the United States between 1973 and 1983 were caused by the vaccine. The CDC also said that every case from 1980 to 1989 was caused by vaccine.
1993 Clinton administration announces plans for a National Childhood Vaccination Program. 103rd Congress introduces S732,S733,HR1460, legislation that would attempt to vaccine all children in the United States, while severely limiting exemptions parents could claim. The bills also seek to set up a national vaccine registry to track down parents who resist.
1993 Seattle Times reports that all polio in the US is caused by vaccines. (6/10/93).
1993 The US Army directs Walter Reed Army Institute of Research to sign an agreement with MicroGeneSys in Meridan, Connecticut for a 'large scale clinical evaluation' of an AIDS vaccine designed to block destruction of the immune system. The VaxSyn vaccine uses a genetically engineered protein that matches a protein called (gp160) that covers the surface of the HIV virus. (Note: That the HIV virus is harmless and does not 'cause AIDS' is known, illustrating that the military is in on the AIDS scam). See Duesberg material.
1994 Researchers at the Gladstone Institute of Virology and Immunology use genetic engineering to alter a Polio virus (Sabin type) to allow it to carry two key genes from the HIV virus, plus proteins from both cholera bacteria and influenza virus, in a misguided attempt to create an 'AIDS vaccine' by induction of immune reaction to foreign proteins. (San Francisco Chronicle 9/2/94)
1994 Sweden reports the testing of a 'new safer Pertussis vaccine' to combat whooping cough (what is now a relatively mild disease). According to an article in The Olympian, Olympia, Washington, it 'could be available in the United States, according to federal health officials.' According to the article 'the vaccine could mean the end of rare, severe side effects associated with the Pertussis/whooping cough vaccine.' (Note: On the contrary, the evidence proves the Pertussis organism found in Pertussis 'vaccine', whether bred in live tissue ('live' virus) or dead tissue ('killed virus'), causes brain damage and other pathology in humans).
1889 Protégé's of Louis Pasteur, Emile Rouz & Alexandre Yersin grew a broth thick with diphtheria bacteria and used compressed air to force the broth through a filter of unglazed porcelain.
NO bacteria or solids could pass through the porcelain - only liquid.
They then sterilized the liquid.
They took the sterilized liquid of diphtheria toxin and injected into animals.
The liquid killed the animals not the bacteria!
According to Dr. Young, this early scientific test showed that a liquid toxic acid kills,not a bacteria or fungi. The major contributors to an acidic body that leads to irritation, inflammation, induration, ulceration and degeneration are as follows:
1) Nitric, sulphuric, phosphoric and uric acids from animal proteins including eggs.
2) Lactic acids from dairy products.
3) All sugars including herbal sugars which are all acids including glucose and ethanol alcohol.
4) Vinegar which is diluted acetylaldehyde an acid that destroys brain cells.
5) All mushrooms and algae which breakdown dead bodies.
6) Peanuts and corn which produce exotoxins and mycotoxins.
7) All fermented foods including soy sauce.
8) Antibiotics which are mycotoxins.
9) Antifungals which are stronger mycotoxins.
10) All vaccinations which are full of exotoxins and mycotoxins.
1994 Dr. Robert O. Young discovers the pH factor in triggering biological transformation of the red blood cells into bacteria and yeast.
1994 Dr. Robert O. Young discovers that there is only one sickness and one disease and that is the over-acidification of the blood and tissues due to an inverted way of living eating and thinking.
1994 to the present the increase of Autism is at epidemic proportions - 1 in 90 boys and 1 in 150 girls are affected. Dr. Young has suggested that this is a result of congestion of the bowels from eating animal proteins and dairy as well as vaccinations and antibiotics that destroys the root system or intestinal villi of the small intestine - the focal point where new blood is produced.
1994 to the present the increase of breast cancers is now 1 in 3 and the increase of prostate cancers in men is now 1 in 2. Dr. Young has suggested that this is a result of antibiotic and anti-fugal use, vaccination and an acidic lifestyle and diet.
2008 A formal investigation has been launched by French authorities against two managers from drug companies GlaxoSmithKline and Sanofi Pasteur. A second investigation for manslaughter has also been opened against Sanofi Pasteur MSD.
The investigations are in response to allegations that the companies failed to fully disclose side effects from an anti-hepatitis B drug used between 1994 and 1998.
During this time, close to two-thirds of the French population, and almost all newborn babies, received a hepatitis B vaccine. The vaccination campaign was halted after concerns rose over the shot's side effects.
Thirty plaintiffs, including the families of five people who died after the vaccination, have launched a civil action in the case against the drug companies. Source: Reuters February 1, 2008
For more information on viruses, bacteria, yeast and vaccines read Sick and Tired, Reclaim Your Inner Terrain, or A Second Thought About Viruses, Vaccines and the HIV AIDS Hypothesis, both by Dr. Robert O. Young.
I would also recommend reading Antione BeChamp's books, The Blood The Third Anatomical Element and The Origin of Organic Beings.
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