That's not proof of anything.No they haven't, as if a study done on mice is somehow "debunked". But once again, why do you think Thimerosal was removed from vaccines? What data were they relying on that showed it to be harmful?
That's not proof of anything.No they haven't, as if a study done on mice is somehow "debunked". But once again, why do you think Thimerosal was removed from vaccines? What data were they relying on that showed it to be harmful?
How do you tell an autistic mouse? Is there even such a thing?No they haven't, as if a study done on mice is somehow "debunked". But once again, why do you think Thimerosal was removed from vaccines? What data were they relying on that showed it to be harmful?
They line up their droppings in careful rows and become very angry when you rearrange them.How do you tell an autistic mouse?
"The most common adjuvant for human use is an aluminum salt called alum derived from aluminum hydroxide, or aluminum phosphate. A quick read of the scientific literature reveals that the neurotoxic effects of aluminum were recognized 100 years ago. Aluminum is a neurotoxicant and has been linked to Alzheimer’s disease and other neurological disorders. Prior to 1980, kidney patients undergoing long term dialysis treatments often suffered dialysis encephalopathy syndrome, the result of acute intoxication by the use of an aluminium-containing dialysate. This is now avoided using modern techniques of water purification. In pre-term infants, prolonged intravenous feeding with solutions containing aluminum is associated with impaired neurologic development. Scientists speculate that aluminum neurotoxicity may be related to cell damage via free radical production, impairment of glucose metabolism, and effects on nerve signal transduction. (2) Vaccines which contain both aluminum adjuvants and mercury based preservative, greatly magnify the neurotoxic effects. (3)
Macrophagic myofasciitis (MMF) is a muscle disease first identified in 1993, and has been linked to vaccines containing aluminum adjuvants. Muscle pain is the most frequent symptom which can be localized to the limbs or be more diffuse. Other symptoms include joint pain, muscle weakness, fatigue, fever, and muscle tenderness. The disorder is associated with an altered immune system in some, but not all patients. A study published in the journal Brain (2001) revealed that 50 out of 50 patients had received vaccines against hepatitis B virus (86%), hepatitis A virus (19%) or tetanus toxoid (58%), 3-96 months (median 36 months) before biopsy. “We conclude that the MMF lesion is secondary to intramuscular injection of aluminum hydroxide-containing vaccines, shows both long-term persistence of aluminum hydroxide and an ongoing local immune reaction, and is detected in patients with systemic symptoms which appeared subsequently to vaccination”, write the authors of the study. (4)
http://www.ovg.ox.ac.uk/vaccine-ingredients#aluminium
Because it was reducing the number of children being vaccinated due to superstition.
If most vaccines were purple, and people thought purple vaccines caused AIDS and thus they avoided them, they'd likely change the color as well. Not because the color of the vaccine means a thing, but because the goals of those organizations are the health of children.
How do you tell an autistic mouse? Is there even such a thing?
The amount of aluminium in the vaccines is about 2 mg.
Utterly harmless.
If you can find some link claiming that such a level of aluminium salt is harmful, please quote it.
Although no evidence suggests that there are safety concerns with thimerosal, vaccine manufacturers have stopped using it as a precautionary measure.
...says the guy who believes in ghosts.You don't know much about scientific research do you?
Yep, agreed with the below part of your post.
At birth, most children are given the hepatitis B vaccination. The amount of aluminum in the Hepatitis B vaccine alone is almost14 TIMES THE AMOUNT OF ALUMINUM THAT IS FDA-APPROVED.
The FDA study found that the maximum amount of aluminum an infant could be exposed to over the first year of life would be 4.225 milligrams (mg), based on the recommended schedule of vaccines. Federal Regulations for biological products (including vaccines) limit the amount of aluminum in the recommended individual dose of biological products, including vaccines, to not more than 0.85-1.25 mg. For example, the amount of aluminum in the hepatitis B vaccine given at birth is 0.25 mg.
Aluminum is found naturally in large quantities in the environment, often consumed through drinking water or ingesting certain foods, such as infant formula. Using the updated parameters, the authors found that the body burden of aluminum from vaccines and diet throughout an infant’s first year of life is significantly less than the corresponding safe body burden of aluminum, based on the minimal risk levels established by the Agency for Toxic Substances and Disease Registry.
Those levels refer to patients with kidney disease, and premature babies.
Here's what the FDA say in an article about this subject:
http://www.fda.gov/BiologicsBloodVaccines/ScienceResearch/ucm284520.htm
"Manufacturers began voluntarily removing Thimerosal from pediatric vaccines around 2000. It is assumed that most pediatric vaccines containing Thimerosal were “off the shelves” by 2003. (No vaccines were recalled.) Even so, most infants are still routinely given Thimerosal-containing influenza vaccine even though there are Thimerosal-free and vaccines with trace amounts of Thimerosal. Infants receiving a Thimerosal-containing influenza vaccine are dosed at 6 months with 12.5 mcg of ethyl mercury and at 7 months with an additional 12.5 mcg. Adult Thimerosal-containing vaccines contain roughly 25mcg. These Thimerosal-containing version exceed federal safety guidelines mentioned earlier.
Depending on the vaccines administered, at six months of age, infants today born to mothers who received flu vaccine during pregnancy could receive up to 71 mcg of ethyl mercury compared to 187.5 mcg prior to efforts to decrease the amount of thimerosal in infant vaccines. Additionally, the new CDC guidelines recommend that all children from 2 to 5 years of age receive an annual influenza vaccine. As a result, the total amount of thimerosal given to children under 5 years of age is almost what it was prior to 2000.
There are other sources of mercury exposure in infants. Specifically, it should be recognized that influenza vaccine recommended for pregnant women and some rhogam preparations contain ethyl mercury in the form of thimerosal. Total mercury burden include other sources including dental amalgams (silver fillings), food especially some types of fish, and air pollution from coal-fired power plants and wildfires.
Concerns regarding mercury in vaccines were addressed in a letter published by the Journal Pediatrics on March 13, 2008.As noted in the letter, parents and pregnant women may want to consider the following data and make an informed decision.
- 0.5 parts per billion (ppb) mercury = Kills human neuroblastoma cells (Parran et al., Toxicol Sci 2005; 86: 132-140).
- 2 ppb mercury = U.S. EPA limit for drinking water.
- 20 ppb mercury = Neurite membrane structure destroyed (Leong et al., Neuroreport 2001; 12: 733-37).
- 200 ppb mercury = level in liquid the EPA classifies as hazardous waste.
- 25,000 ppb mercury = Concentration of mercury in the Hepatitis B vaccine, administered at birth in the U.S., from 1990-2001.
- 50,000 ppb Mercury = Concentration of mercury in multi-dose DTaP and Haemophilus B vaccine vials, administered 4 times each in the 1990's to children at 2, 4, 6, 12 and 18 months of age.
- 50,000 ppb Mercury = Current "preservative" level mercury in multi-dose flu (94% of supply), meningococcal and tetanus (7 and older) vaccines. This can be confirmed by simply analyzing the multi- dose vials."===http://www.nvic.org/faqs/mercury-thimerosal.aspx
It's not free murcury, it's a compound. Not the same thing.I don't like to see that the flu shot has that much mercury in it. What is the reasoning here? I'm not convinced that any amount of mercury is safe.
Would have been more interesting if they had extended the data past 1998 to see if it held in reverse: IE, since mercury has been phased-out, did new autism cases also plummet?Interesting chart:
That statement says nothing about "high mercury levels in infants". In fact, it explicitly states that no evidence of a health risk exists. You're either lying (yet, with the truth in plain English right in front of you?) or you have a severe reading comprehension problem.Uh no. It was because given all the other sources of mercury in our environment, it was important to reduce high mercury levels in infants induced by vaccines. Here's the CDC's statement:
It's not free murcury, it's a compound. Not the same thing.
Now I have to find out if the flu shot my 4 year old just got had thimerosal in it. I was under the impression that it was no longer in vaccines. I will also forward that study to see what he thinks.But it ends up as the same after metabolizing:
"The vaccine purveyors often argue that “ethylmercury” compounds (THIMEROSAL) are safe, while admitting that “methylmercury” compounds are harmful. Hence industry uses the FDA-approved purportedly “safe” ethlymercury compound found in Thimerosal.
Having thoroughly reviewed two key published studies on mercury metabolism, one in rats and one in human infants, what Dr. Paul G. King noticed and articulated, among other realities, in his latest posting is that during the metabolic process in the human and animal bodies the supposedly “harmless” ethylmercury compound, Thimerosal, is metabolized (converted) into the toxic and “harmful” methylmercury. And then in turn, the harmful methylmercury is metabolized (converted) into the most harmful, long-term-toxic, “inorganic” mercury that is retained in bodily tissues.
In the rat study, which Dr. King cites, the lab rats were raised for the purpose of this study and had no reported mercury levels in their blood before the experiment.
There were three groups in the study:
1. A test group of Thimerosal-(ethylymercury)-treated rats;
2. A test group of methylmercury-chloride-treated rats; and
3. A control group of rats treated with a ‘water’ placebo.
At the end of the experiment, as expected, the water-treated control group had no reported levels of mercury in their blood or organs.
The group treated with methylmercury chloride (which vaccine purveyors routinely “sound bite” as the harmful organic mercury as compared to the “safe” Thimerosal, ethylmercury), as expected, had both methylmercury and inorganic mercury in their blood and organs.
Note: “Inorganic” mercury is the end product of mercury metabolism. The methylmercury subject group confirmed that the metabolic pathway for mercury in the human and animal body consists in the reduction/conversion of the harmful methylmercury into a more harmful “inorganic” mercury which is tissue-bound, and long-term-toxic. Hence, both the originating substance (methylmercury) and its conversion/reduction, inorganic mercury was found.
The Thimerosal Group: Unexpectedly, the rats treated with Thimerosal (ethylmercury) were found to have three types of mercury in the blood samples and their organs, ethylmercury (the originating “supposedly harmless” compound), methylmercury (the admittedly harmful compound) and inorganic mercury (the most harmful, tissue bound end product of mercury metabolism).
This observation begs an answer to the question: Where did the “methylmercury” come from since this group was only originally and solely treated with Thimerosal (an “ethylmercury” compound)?
Based on the published findings in the three groups of rats, the metabolic pathway for organic mercury involves the conversion of Ethylmercury (Thimerosal) into “methylmercury” and then the further reduction of “methylmercury” into inorganic mercury.
It may be that some of the “ethylmercury” (from Thimerosal) are also directly converted into inorganic mercury. However, there are apparently no studies, in either humans or other animals, that establishes the biochemical conversion of ethylmercury compounds directly into the “inorganic” mercury.
In conclusion, in simple layman’s terms, these studies, as brought to light by Dr. King, establish that ethylmercury (Thimerosal), a “supposedly harmless” compound of mercury according to the vaccine establishment, is converted in the rat [1] and apparently in the human infant [2] into “methylmercury” which, the establishment admits is a harmful form of mercury. It is then further reduced to the long-term most harmful, “inorganic mercury” that bioaccumulates in the tissues and organs.
Based on these findings, we can conclude that injecting the Thimerosal (ethylmercury), found in flu shots, into pregnant women (exposing the in utero fetus to mercury [see Table I on page 15 of Dr. King’s posting (http://dr-king.com/docs/110915_PGKReviewOfUSSubmissionToUNEP_b.pdf)] and the egregious recommendation that children should be vaccinated, annually with Thimerosal-preserved inactivated-influenza vaccines from 6 months of age until 18 years of age is a perplexing interwoven government/pharmaceutical health strategy that afflicts, debilitates and destroy the lives of individuals and their families in the United States (US) and in any other nation that: a) recommends inactivated-influenza vaccines for pregnant women and children, b) permits those flu shots to be Thimerosal-preserved and c) follows the US recommendations for annual flu shots.
P.S. One more interesting observation: At sacrifice, the rats in the group that had been treated with Thimerosal-ethylmercury (supposed the harmless compound) had significantly higher levels of the long-term, harmful “inorganic” mercury in their brains than the rats in the methylmercury-chloride-treated group.
Perhaps we should inject the harmful methylmercury directly into our children’s arms instead of Thimerosal (ethylmercury). It appears that if we use the harmful form of mercury right off the bat, there is less inorganic mercury in our children’s brains. But, on the other hand, if the establishment wants more inorganic mercury in our children’s brains and organs (which it appears they do) lets stick with Thimerosal. The pharmaceutical companies stand to gain when we make our children sicker and sicker by injecting them first in-utero and then consistently, year after year, with a known and extremely dangerous neurotoxin. And both the government and the pharmaceutical companies stand to gain when they injury the emerging generation with vaccines, misdiagnose them as mentally ill (Autistic, ADD, ADHD, Biopolar, OCD, etc.) and then dumb them down with a life long supply of psyche drugs which, according to the Mayo Clinic is resulting in the birth of an epidemic of deformed offspring.
References:
[1]Rodriques JL, Serpeloni JM, Batista BL, Souza S, Barbosa Jr F. Identification and distribution of mercury species in rat tissues following administration of Thimerosal or methyl mercury. Arch Toxicol 2010; 84: 891-896.
[2]Pichichero ME, Gentile A, Giglio N, Umido V, Clarkson T, Cernichiari E, Zareba G, Gotelli C, Gotelli M, Yan L, and Treanor J. (2008) Mercury Levels in Newborns and Infants After Receipt of Thimerosal-Containing Vaccines. Pediatrics 2008; 121(2): e208-e214."===http://www.infowars.com/establishme...ccines-vs-admittedly-dangerous-methylmercury/