For Dr. Fudenberg's proof I would suggest you check into his papers: Hazards of Vaccines 1 & 2 in Internat. J. Clin. Invest., 2000 & 2004.

My suspicions are that even if, as you say, "mercury from vaccinations clears the human body very rapidly," there is the problem of synergy. In the presence of aluminum, mercury becomes a hundred times more toxic. There is aluminum in vaccinations as well.

http://www.foodintegrity.com

What proof do you have that mercury clears the human body very rapidly? From what I have read some people may be able to eliminate the mercury in their bodies in three years without chelation but even they may never eliminate the mercury in their brain without chelation. To my knowledge there are no human studies on mercury IN the human body in living people. You can test for mercury being excreted though. There has never been a test to find out how much mercury is excreted after vaccination. There is no way to test for mercury in a persons brain unless you remove a portion of the brain.

Mercury on the Mind
by Donald W. Miller, Jr., MD
by Donald W. Miller, Jr., MD


Autism was discovered in 1943, in American children, twelve years after ethyl mercury (thimerosal) was added to the pertussis vaccine. (The disease was not seen in Europe until the 1950s, after thimerosal was added to vaccines used there.) In a typical case, shortly before his 2nd birthday a normally developing, healthy boy stops communicating with others and withdraws into himself. He avoids eye contact and becomes strange and aloof. His vision becomes blurred; and he develops various motor disturbances, such as involuntary jerking of the arms and legs and walking on his toes. In addition to these manifestations, Dr. Sallie Bernard and her colleagues, in a study titled, ""http://www.vaccinationnews.com/DailyNews/July2001/AutismUniqueMercPoison.htm"," describe the speech difficulties, unusual behavior (such as unprovoked crying spells and head banging), various degrees of cognitive impairment, gastrointestinal difficulties, and immune difficulties that these autistic children can have. Mercury is most likely a causative factor in other developmental disorders as well, such as delayed speech and attention deficit hyperactivity disorder.
"http://www.medscimonit.com/pub/vol_10/no_3/3986.pdf" that there is a direct relationship between increasing doses of mercury in vaccines and autism. In the 1950s, with an immunization schedule limited to four vaccines (against diphtheria, tetanus, pertussis, and smallpox), 1 in 10,000 children developed this disease. As vaccines for other diseases were added, health care providers began injecting increasingly larger doses of mercury into children. Those born in 1981 were given 135 micrograms of mercury (on average), and one case of autism occurred in every 2,600 children born that year. With the addition of hepatitis B vaccine (injected on the day of birth) and one for Haemophilus influenzae Type b, providers injected 246 micrograms of mercury into children born in 1996. Autism occurred in one out of every 350 of these children. Today, providers follow an "http://www2a.cdc.gov/nip/scheduler_le/schedule.asp", prepared by the CDC and approved by the AAP and AAFP, that includes 13 vaccines given, with variable numbers of booster shots, 33 times before a child reaches the age of 2 (when the development of the brain is completed). Autism now afflicts 1 in 100 boys and 1 in 400 girls, and physicians diagnose 100,000 new cases of this disease every year in the U.S (using diagnostic criteria, in the DSM-IV, that is more restrictive than the previous DSM-IIIR). Over the last 30 years more than one million children have come down with this disease, and currently one in every 68 families in America has an autistic child.
Mainstream medical journals, like Pediatrics and The New England Journal of Medicine, only publish studies that claim thimerosal is safe. And it turns out that these articles are written in large part by researchers in the pay of vaccine makers, as the "http://www.safeminds.org/" (Sensible Action For Ending Mercury-Induced Neurological Disorders), a private nonprofit organization, "http://www.safeminds.org/pressroom/press_releases/20040518_AutismAuthorsNetwork.pdf". Editors of these journals will not publish studies that show a link between thimerosal and autism like ""http://www.jpands.org/vol8no1/geier.pdf"" by Mark and David Geier, which documents a strong association between the amounts of mercury injected in vaccines and autism. Such articles can only find acceptance in alternative (i.e., "politically incorrect") journals like the "http://www.jpands.org/", where this one was published.
The amount of damage a given dose of mercury can do to the brain (and also the heart) depends on one’s age, sex, and genetically determined ability to excrete mercury. Young children with still developing brains are more susceptible, and males are more vulnerable to a given dose of mercury because testosterone enhances its neurotoxicity. Most important, however, is one’s genetically programmed ability to rid the body of mercury. The brain has a house-cleaning protein that removes dangerous waste products, which comes in three varieties: APO-E2, APO-E3, and APO-E4. The APO-E2 protein can carry 2 atoms of mercury out of the brain; APO-3, one; and AOP-E4, none. The genes we acquire from each parent determine which two we have. People with two APO-E4 proteins (and thus no APO-E2 or -E3) have an 80 percent chance of acquiring Alzheimer’s disease. And according to one study, autistic children have a huge preponderance of APO-E4 protein in their brains.
Alzheimer’s disease was discovered in 1906, again in America, where dentists used mercury-laden Amalgams to fill cavities (dentists in Europe largely avoided them). Today, more than 4 million Americans now have Alzheimer’s disease. It afflicts half of people over the age of 85 and 20 percent aged 75 to 84.
The first symptoms of this disease are difficulty concentrating and variable degrees of memory loss, leading ultimately to devastating mental deterioration. The brains of people with Alzheimer’s disease shrink by 25 percent and have distinct pathologic hallmarks (neurofibillary tangles, amyloid plaques, and phosphorylation of tau protein). Brain cells grown in the laboratory develop the same three pathologic findings when exposed to nanomolar (3.6 × 10-10 molar) doses of mercury, an amount approximating that found in the brains of people who have a lot of Amalgam fillings.
Dental Amalgams are the main source of mercury in an adult’s brain. An average-sized Amalgam filling contains 750,000 micrograms of mercury and releases around 10 micrograms a day. Researchers put radiolabelled mercury Amalgams in the teeth of sheep and determined where escaped mercury went with a scanner. They showed that mercury atoms exhaled through the nose travel up filaments of the olfactory nerve to the hippocampus, which controls memory, and to other critical areas in the brain. In another "http://www.holistic-dentistry.com/artalzeimer.asp", rats given the same concentration of mercury that people inhale from their amalgams develop the pathologic markers of Alzheimer’s disease. People with Alzheimer’s disease have mercury levels in their brains that are 2 to 3 times higher than that seen in normal people.
The mercury in flu vaccines also plays a role in this disease. One investigator "http://suewidemark.freeservers.com/flushot-alzheimers.htm" that people who received the flu vaccine each year for 3 to 5 years had a ten-fold greater chance of developing Alzheimer’s disease than people who had zero, 1, or 2 shots.
Another important factor with regard to mercury on the mind, which officials at the CDC, FDA and the professors in the IOM do not consider, is "http://www.talkinternational.com/health/report_on_mercury_toxicity_bh_050803.htm" – mercury’s enhanced effect when other poisons are present. A small dose of mercury that kills 1 in 100 rats and a dose of aluminum that will kill 1 in 100 rats, when combined have a striking effect: all the rats die. Doses of mercury that have a 1 percent mortality will have a 100 percent mortality rate if some aluminum is there. Vaccines contain aluminum.


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What proof do you have that mercury clears the human body very rapidly? To my knowledge there are no human studies on mercury IN the human body in living people. You can test for mercury being excreted though. There has never been a test to find out how much mercury is excreted after vaccination. There is no way to test for mercury in a persons brain unless you remove a portion of the brain.

Mercury on the Mind
by Donald W. Miller, Jr., MD
by Donald W. Miller, Jr., MD


Autism was discovered in 1943, in American children, twelve years after ethyl mercury (thimerosal) was added to the pertussis vaccine. (The disease was not seen in Europe until the 1950s, after thimerosal was added to vaccines used there.) In a typical case, shortly before his 2nd birthday a normally developing, healthy boy stops communicating with others and withdraws into himself. He avoids eye contact and becomes strange and aloof. His vision becomes blurred; and he develops various motor disturbances, such as involuntary jerking of the arms and legs and walking on his toes. In addition to these manifestations, Dr. Sallie Bernard and her colleagues, in a study titled, ""http://www.vaccinationnews.com/DailyNews/July2001/AutismUniqueMercPoison.htm"," describe the speech difficulties, unusual behavior (such as unprovoked crying spells and head banging), various degrees of cognitive impairment, gastrointestinal difficulties, and immune difficulties that these autistic children can have. Mercury is most likely a causative factor in other developmental disorders as well, such as delayed speech and attention deficit hyperactivity disorder.
"http://www.medscimonit.com/pub/vol_10/no_3/3986.pdf" that there is a direct relationship between increasing doses of mercury in vaccines and autism. In the 1950s, with an immunization schedule limited to four vaccines (against diphtheria, tetanus, pertussis, and smallpox), 1 in 10,000 children developed this disease. As vaccines for other diseases were added, health care providers began injecting increasingly larger doses of mercury into children. Those born in 1981 were given 135 micrograms of mercury (on average), and one case of autism occurred in every 2,600 children born that year. With the addition of hepatitis B vaccine (injected on the day of birth) and one for Haemophilus influenzae Type b, providers injected 246 micrograms of mercury into children born in 1996. Autism occurred in one out of every 350 of these children. Today, providers follow an "http://www2a.cdc.gov/nip/scheduler_le/schedule.asp", prepared by the CDC and approved by the AAP and AAFP, that includes 13 vaccines given, with variable numbers of booster shots, 33 times before a child reaches the age of 2 (when the development of the brain is completed). Autism now afflicts 1 in 100 boys and 1 in 400 girls, and physicians diagnose 100,000 new cases of this disease every year in the U.S (using diagnostic criteria, in the DSM-IV, that is more restrictive than the previous DSM-IIIR). Over the last 30 years more than one million children have come down with this disease, and currently one in every 68 families in America has an autistic child.
Mainstream medical journals, like Pediatrics and The New England Journal of Medicine, only publish studies that claim thimerosal is safe. And it turns out that these articles are written in large part by researchers in the pay of vaccine makers, as the "http://www.safeminds.org/" (Sensible Action For Ending Mercury-Induced Neurological Disorders), a private nonprofit organization, "http://www.safeminds.org/pressroom/press_releases/20040518_AutismAuthorsNetwork.pdf". Editors of these journals will not publish studies that show a link between thimerosal and autism like ""http://www.jpands.org/vol8no1/geier.pdf"" by Mark and David Geier, which documents a strong association between the amounts of mercury injected in vaccines and autism. Such articles can only find acceptance in alternative (i.e., "politically incorrect") journals like the "http://www.jpands.org/", where this one was published.
The amount of damage a given dose of mercury can do to the brain (and also the heart) depends on one’s age, sex, and genetically determined ability to excrete mercury. Young children with still developing brains are more susceptible, and males are more vulnerable to a given dose of mercury because testosterone enhances its neurotoxicity. Most important, however, is one’s genetically programmed ability to rid the body of mercury. The brain has a house-cleaning protein that removes dangerous waste products, which comes in three varieties: APO-E2, APO-E3, and APO-E4. The APO-E2 protein can carry 2 atoms of mercury out of the brain; APO-3, one; and AOP-E4, none. The genes we acquire from each parent determine which two we have. People with two APO-E4 proteins (and thus no APO-E2 or -E3) have an 80 percent chance of acquiring Alzheimer’s disease. And according to one study, autistic children have a huge preponderance of APO-E4 protein in their brains.
Alzheimer’s disease was discovered in 1906, again in America, where dentists used mercury-laden amalgams to fill cavities (dentists in Europe largely avoided them). Today, more than 4 million Americans now have Alzheimer’s disease. It afflicts half of people over the age of 85 and 20 percent aged 75 to 84.
The first symptoms of this disease are difficulty concentrating and variable degrees of memory loss, leading ultimately to devastating mental deterioration. The brains of people with Alzheimer’s disease shrink by 25 percent and have distinct pathologic hallmarks (neurofibillary tangles, amyloid plaques, and phosphorylation of tau protein). Brain cells grown in the laboratory develop the same three pathologic findings when exposed to nanomolar (3.6 × 10-10 molar) doses of mercury, an amount approximating that found in the brains of people who have a lot of Amalgam fillings.
Dental amalgams are the main source of mercury in an adult’s brain. An average-sized amalgam filling contains 750,000 micrograms of mercury and releases around 10 micrograms a day. Researchers put radiolabelled mercury amalgams in the teeth of sheep and determined where escaped mercury went with a scanner. They showed that mercury atoms exhaled through the nose travel up filaments of the olfactory nerve to the hippocampus, which controls memory, and to other critical areas in the brain. In another "http://www.holistic-dentistry.com/artalzeimer.asp", rats given the same concentration of mercury that people inhale from their amalgams develop the pathologic markers of Alzheimer’s disease. People with Alzheimer’s disease have mercury levels in their brains that are 2 to 3 times higher than that seen in normal people.
The mercury in flu vaccines also plays a role in this disease. One investigator "http://suewidemark.freeservers.com/flushot-alzheimers.htm" that people who received the flu vaccine each year for 3 to 5 years had a ten-fold greater chance of developing Alzheimer’s disease than people who had zero, 1, or 2 shots.
Another important factor with regard to mercury on the mind, which officials at the CDC, FDA and the professors in the IOM do not consider, is "http://www.talkinternational.com/health/report_on_mercury_toxicity_bh_050803.htm" – mercury’s enhanced effect when other poisons are present. A small dose of mercury that kills 1 in 100 rats and a dose of aluminum that will kill 1 in 100 rats, when combined have a striking effect: all the rats die. Doses of mercury that have a 1 percent mortality will have a 100 percent mortality rate if some aluminum is there. Vaccines contain aluminum.