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Originally posted by Blaine91555
reply to post by jameshawkings
We also have the fact that Whooping Cough, a horror I went through as a child that should not exist today is making a comeback. It coincides exactly with Parents suddenly deciding to not vaccinate their children. Strong evidence it seems to me. Should be an alarm bell to the Parents who doomed their own children to catching it based on radical views expressed by people pushing a personal agenda like the so called anonymous person in the interview. In this conspiracy topic their are and will be real victims, including dead children that should be alive.
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Originally posted by liveyourlife
I know people will argue the autism case on this....but there could be many other factors that are causing the increase in autistic children, such better diagnosis procedures, pollution, genetics...it goes on and on.
Originally posted by VneZonyDostupa
reply to post by dfens
I did attack the "meat of the post". Your "meat" demanded that I prove a negative rather than asking for proof of a positive. This is illogical. When someone makes a claim ("most researchers have financial conflicts of interest" in Soficrow's case), why SHOULDN'T he have to prove that claim? Why should I have to prove his statement ISN'T true, rather than just asking him to support the original statement?
The point of this web site, and in fact the web site's motto, is to "deny ignorance". Making sweeping claims, such as claiming "most researchers" doe X or Y, without any tangible proof, is the antithesis of denying ignorance.edit on 1/19/2011 by VneZonyDostupa because: (no reason given)
THE revelation that the diabetes drug Avandia can potentially cause heart disease is the latest in a string of pharmaceutical disappointments. Vioxx was pulled from the market in 2004 because it doubled the risks for heart attacks and strokes. Eli Lilly recently paid $750 million to settle lawsuits alleging that Zyprexa causes diabetes. Many have criticized the Food and Drug Administration as being too lax about monitoring drug safety.
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The great majority of “new” drugs are not new at all but merely variations of older drugs already on the market. These are called “me-too” drugs. The idea is to grab a share of an established, lucrative market by producing something very similar to a top-selling drug. For instance, we now have six statins (Mevacor, Lipitor, Zocor, Pravachol, Lescol, and the newest, Crestor) on the market to lower cholesterol, all variants of the first. As Dr. Sharon Levine, associate executive director of the Kaiser Permanente Medical Group, put it,
Over the past two decades the pharmaceutical industry has moved very far from its original high purpose of discovering and producing useful new drugs. Now primarily a marketing machine to sell drugs of dubious benefit, this industry uses its wealth and power to co-opt every institution that might stand in its way, including the US Congress, the FDA, academic medical centers, and the medical profession itself. (Most of its marketing efforts are focused on influencing doctors, since they must write the prescriptions.)
The most important of these laws is known as the Bayh-Dole Act, after its chief sponsors, Senator Birch Bayh (D-Ind.) and Senator Robert Dole (R-Kans.). Bayh-Dole enabled universities and small businesses to patent discoveries emanating from research sponsored by the National Institutes of Health, the major distributor of tax dollars for medical research, and then to grant exclusive licenses to drug companies.
Faculty researchers were encouraged to obtain patents on their work (which were assigned to their universities), and they shared in the royalties. Many medical schools and teaching hospitals set up “technology transfer” offices to help in this activity and capitalize on faculty discoveries. As the entrepreneurial spirit grew during the 1990s, medical school faculty entered into other lucrative financial arrangements with drug companies, as did their parent institutions.
(NaturalNews) It's being called the largest research fraud in medical history. Dr. Scott Reuben, a former member of Pfizer's speakers' bureau, has agreed to plead guilty to faking dozens of research studies that were published in medical journals.
Now being reported across the mainstream media is the fact that Dr. Reuben accepted a $75,000 grant from Pfizer to study Celebrex in 2005. His research, which was published in a medical journal, has since been quoted by hundreds of other doctors and researchers as "proof" that Celebrex helped reduce pain during post-surgical recovery. There's only one problem with all this: No patients were ever enrolled in the study!
Source
It's times like these when I'm happy that I haven't published in too many Elsevier Journals during the course of my career. I say that because on Thursday, it was revealed that pharmaceutical company Merck, Sharp & Dohme paid Elsevier to produce a fake medical journal that, to any superficial examination, looked like a real medical journal but was in reality nothing more than advertising for Merck. As reported by The Scientist:
Scienceblog
Originally posted by VneZonyDostupa
reply to post by soficrow
So, you have no evidence that "most researchers" have financial conflicts? Is that what I'm supposed to draw from your post? All I see is a revision of guidelines, which happens all the time to accommodate changing technology, trends, and environments.
Why can't you just provide evidence of your claim, rather than dancing around the point?
Why bother to call attention to Dr. Paul Offit, the vaccine patent-holder who has led the attack on the idea that vaccines have anything to do with autism or any of the myriad of other ailments afflicting this generation of American children? Well, because other people are paying attention -- including the nation's pediatricians and the mainstream journalists who need to start calling him to account. Offit has a new book out -- "Deadly Choices: How the Anti-Vaccine Movement Threatens Us All." Here's the question doctors who recommend him to nervous parents, and parents unsure what to think, and journalists who interview him, need to ask: Why is Offit transparently opposed to ever studying the health outcomes of vaccinated versus unvaccinated Americans, even as he acknowledges that vaccines have a long history of causing serious side effects?
While his last book, "Autism's False Prophets," focused squarely on the disability now afflicting 1 in 100 children, Offit branches out here to deride those who have any concerns whatsoever about the safety of the current vaccine schedule. There is plenty of sympathy for parents of children who have died of infectious diseases, but perfunctory dismissal in cases where parents blame vaccines.
Dr. Offit shares the patent on the Rotavirus vaccine in development by Merck and lists a $350,000 grant from Merck for Rotavirus vaccine development. Also, he lists that he is a consultant to Merck.
c. Dr. Paul Offit
Dr. Offit lists that he is a consultant to Merck on an attachment to his OGE 450, but does not disclose whether or not he received any remuneration for his services. (Exhibit 39)
Dr. Offit began his tenure on ACIP in October of 1998. Out of four votes pertaining to the ACIP’s rotavirus statement he voted “yes” three times, including, voting for the inclusion of the rotavirus vaccine in the VFC program.
Dr. Offit abstained from voting on the ACIP’s rescission of the recommendation of the rotavirus vaccine for routine use. He stated at the meeting, “I’m not conflicted with Wyeth, but because I consult with Merck on the development of rotavirus vaccine, I would still prefer to abstain because it creates a perception of conflict.”
[lxvii] In the hearings in the House
He was questioned continually by Dan Burton, Congressman in the Conflict of Interest Hearings in D.C. about his conflicts and he ABSOLUTELY denied that the above made a conflict because he was an honest man.
The use of a combination vaccine generally is preferred over separate injections of its equivalent component vaccines.
Originally posted by liveyourlife
I have to say I find it a little frightening that people do not have their children vaccinated. The purpose is to prevent your child from contracting a disease that will hurt them, possibly for the rest of their lives or kill them. It is also to prevent the spread of disease to others. This is why we there is not wide spread cases of mumps or polio. I dont know if you have ever seen a picture of someone who has the mumps, but I would never forgive myself if my child contracted that disease because I did not make sure they were vaccinated.
I know people will argue the autism case on this....but there could be many other factors that are causing the increase in autistic children, such better diagnosis procedures, pollution, genetics...it goes on and on.
Mercury concentrations in brain and kidney following ethylmercury, methylmercury and Thimerosal administration to neonatal mice
G. Jean Harrya, , , Martha W. Harrisb and Leo T. Burkac
aLaboratory of Neurobiology, Neurotoxicology Group, National Institute of Environmental Health Sciences, P.O. Box 12233, MD C1-04, Research Triangle Park, NC 27709, USA
bLaboratory of Molecular Toxicology, National Institute of Environmental Health Sciences, National Institutes of Health, Health and Human Services, Research Triangle Park, NC 27709, USA
cLaboratory of Pharmacology and Chemistry, National Institute of Environmental Health Sciences, National Institutes of Health, Health and Human Services, Research Triangle Park, NC 27709, USA
Received 8 June 2004; revised 28 July 2004; accepted 28 July 2004. Available online 18 September 2004.
Abstract
The distribution of mercury to the brain following an injection of methylmercury (MeHg) or ethylmercury (EtHg) was examined in immature mice. Postnatal day (PND) 16 CD1 mice received MeHg chloride either by IM injection or by gavage. At 24 h and 7 days post-injection, total mercury concentrations were determined in blood, kidney, brain, and muscle by cold vapor atomic fluorescence spectrometry. At 24 h, an IM injection of MeHg chloride (17.4 μg) produced total mercury concentrations in the blood (6.2 ± 0.9 μg/g), brain (5.6 ± 1.3 μg; 0.6% delivered dose), and kidney (25.2 ± 5.6 μg; 1.1%), approximately 30% of that obtained from oral administration (blood: 17.9 ± 1.0 μg; brain: 16.1 ± 1.2 μg, 1.5%; kidney: 64.9 ± 6.3 μg, 2.7%). For comparison, PND 16 mice received an IM injection of concentrated dosing suspensions (2 μl dosing vol.) for EtHg chloride (6 μg) or Thimerosal (15.4 μg). For EtHg, approximately 0.39 ± 0.06% of the injected mercury was detected in the brain and 3.5 ± 0.6% in the kidney at 24 h. Thimerosal IM injection resulted in 0.22 ± 0.04% in the brain, and 1.7 ± 0.3% in the kidney. By 7 days, mercury levels decreased in the blood but were unchanged in the brain. An acute IM injection to adult mice of each suspension at a 10-fold higher dose resulted an average 0.1% mercury in the brain, and higher levels in the blood, kidney, and muscle as compared to the young. In immature mice, MeHg delivered via oral route of administration resulted in significantly greater tissue levels as compared to levels from IM injection. Comparisons of tissue distribution following IM administration suggest that an oral route of administration for mercury is not comparable to an IM delivery and that MeHg does not appear to be a good model for EtHg-containing compounds.
Keywords: Thimerosal; Mercury; Tissue distribution
Originally posted by kalamatas
And you simply LIE about the ethyl mercury not being able to reach the brain: