E-News: Burton Demands Recall of Vaccines with Mercury

xmlns:o="urn:schemas-microsoft-com:office:office" xmlns:w="urn:schemas-microsoft-com:office:word" xmlns="http://www.w3.org/TR/REC-html40"> E-News:  Burton Demands Recall of Vaccines with Mercury

E-NEWS FROM THE NATIONAL VACCINE INFORMATION CENTER

Vienna, Virginia                                    http://www.909shot.com “Protecting the health and informed consent rights of children since 1982.”

Subject:    Chairman Burton on House Floor May 15

                  INSTANT RECALL ON ANY VACCINE GOING INTO OUR CHILDREN THAT HAS MERCURY IN

                  IT - (House of Representatives - May 15, 2001)

 [Page:      H2174]

 

The SPEAKER pro tempore. Under a previous order of the House, the gentleman from Indiana (Mr. BURTON) is recognized for 5 minutes.  Mr. BURTON of Indiana. Mr. Speaker, I had a prepared statement that I was going to use, but it has not arrived, so I will speak extemporaneously tonight.

Mr. Speaker, vaccinations have been a real plus for this country. We had a lot of diseases that used to be so feared, like polio and diptheria that we do not have to worry about anymore, and it is because we have vaccinations that really help protect our young people.

But along with the positives, unfortunately there are some negatives, and parents across this country ought to be aware of the negatives as well as the positives. That is why my committee has been holding a number of hearings and has had the health agencies of this country before the committee numerous times.

We have had what is called an explosion of autism in America. Autism, that is a disease most people are not familiar with unless it has hit their family, and that is where one day your child is apparently normal or appears to be normal, and the next day he is running around flapping his arms, cannot speak clearly anymore, bangs his head against the wall, has severe bowel disorders and other related things.

We have had an explosion, an absolute explosion. Twenty years ago, 1 in 10,000 children in America were considered autistic.

Today it is 1 in 500. In some parts of the country, it is as many as 1 in 150. Now think about that; 1 in 150 children in some parts of this country is autistic. We need to find out why.

Our committee has held hearings, and we think we have some things that need to be thoroughly investigated, and one of those is why do we have vaccines going into children’s arms and into adults arms that contain mercury.  Mercury.

Mercury is a toxic substance that we have taken out of our topical dressings. It used to be that you could buy creams that had mercury in them because it was a preservative. They said because it could leach into the bloodstream through the skin, they thought it was safer to take it out of all topical dressings. They still use it as a preservative in many of the vaccinations given to our children.

Mercury is being injected, as I speak tonight, into children across this country along with the vaccinations they are getting.

Other substances being injected into our children are formaldehyde and aluminum, metals that could be and substances that could be toxic. We need to find out why.

I, for one, believe that my grandson became autistic at least in part because he received vaccinations. He received 9 in 1 day,  and 6 of those contained mercury. Mercury has a cumulative effect in the body. It gets in the brain. So I believe that 1 week after he received these vaccinations, he became autistic.

He spoke normally. He acted like any other normal child. Yet within 1 week he was running around flapping his arms, walking on his toes, because he had severe bowel disorder, banging his head against the wall, and he could not speak clearly anymore, and he still has those problems.

Mr. Speaker, if what we are putting into our children’s bodies along with the vaccinations is causing that, something has to be done.  I asked the Food and Drug Administration when they were before our committee, do we have vaccines that do not contain mercury or these substances? They said, yes, we do, in single-vial doses. Now, what does that mean? It means that if we have single-vial doses that do not contain the mercury, the child is not going to get the mercury.

But what happens is, the pharmaceutical companies are putting out many shots into one vial, and because of that they have to have these preservatives in there, and in many cases they put several vaccines together. And so they have these preservatives in there to make sure that the vaccine does not become contaminated.

If we went to single-vial vaccines and shots, we would eliminate, in my opinion, a large part of the problem. But that is why this country needs to have continued oversight over our health agencies, because our health agencies have not really been following up on these vaccines to find out if there are any side effects that are really going to hurt our kids for the rest of their lives.

Mr. Speaker, I will say tonight that mercury should be taken out of every vaccine in the country, and it should be taken out today. There should be an instant recall on any vaccine that is going into our children that has mercury in it.

We have enough vaccines that do not contain these toxic chemicals and substances, so our children can be inoculated in a safe and effective way, and yet our health agencies continue to let these companies use mercury in these vaccines.

Today as I speak, as I said, children are being vaccinated with these toxic chemicals in them. It is unconscionable.

Mr. Speaker, we have what is called SIDS deaths, and they have said it is because children go to bed and they sleep on the wrong side, and there is no explanation why they do not. My granddaughter received a Hepatitis B shot, and within an hour she quit breathing. We had to you rush her to the hospital, and she was blue in the face.

Had she been in bed, the next morning she would have been dead; but my daughter saw her and saw her turning blue and rushed her to the hospital. It was a reaction to the Hepatitis B shot.

Mr. Speaker, let me just say in conclusion, we will have more of these 5-minute special orders, every parent in the country ought to start reading the inserts on those vaccines. Vaccinations are important, but we want to make sure we know what is going into our children’s bodies.  [Begin Insert]

COMMITTEE ON GOVERNMENT REFORM’S OVERSIGHT ACTIVITIES OF VACCINE SAFETY

During the 106th Congress the Full Government Reform Committee and two of its Subcommittees initiated investigations looking at several vaccine issues. There are increasing concerns that the risks related to vaccines are not widely known or acknowledged.

Vaccines have been hailed as the greatest public health advance in the twentieth century. I have said from the outset of our investigation that I am not anti-vaccine . Rather I support the appropriate use of safe vaccines that have been thoroughly tested. I support improved information sharing with parents and patients regarding the benefits and risks of immunization and respect the concerns that have been raised by thousands of families across the United States about vaccine adverse events. I also support increased clinical research looking at the long-term safety of vaccines, including their potential link to chronic conditions such as autism, diabetes, attention-deficit disorder, and asthma.

Vaccines are the only drugs Americans are mandated to receive as a condition of attendance at day care and schools and in some cases as a condition of employment. Because each state bases its mandatory immunizations on Federal recommendations, it is very important that adequate oversight be provided by Congress to insure the integrity of the vaccine programs.  At this time, there is a paucity of research looking at long-term safety of any vaccine . This was acknowledged last year in a report to Congress from the Institute of Medicine, “Few vaccines for any disease have been actively monitored for adverse effects over long periods of time.

CONFLICT OF INTEREST ON VACCINE -RELATED ADVISORY COMMITTEES

The Committee investigated two vaccine -related advisory committees. We were

concerned that the pharmaceutical industry has too much influence over these

committees. From the evidence we found, I think they do. The first committee

was the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC). This Committee makes recommendations on whether new vaccines should be licensed. The second committee is the CDC’s Advisory Committee on Immunizations Practices (ACIP). This committee recommends which vaccines should be included on the Childhood Immunization Schedule. We focused on the handling of the rotavirus vaccine . The FDA approved it for use in August 1998. The CDC recommended it for universal use in March 1999. Serious problems cropped up shortly after it was introduced. Children started developing serious bowel obstructions. The vaccine was pulled from the U.S.  market in October 1999. We learned that during the FDA’s committee meetings there was concern raised about adverse events. They were aware of potential problems. Five children out of 10,000 developed bowel obstructions. There were also concerns about children failing to thrive and developing high fevers, which as we know from other vaccine hearings, can lead to brain injury. Even with all of these concerns, the committee voted unanimously to approve it.

At the CDC’s committee, there was a lot of discussion about whether the benefits of the vaccine really justified the costs. Even though the cost-benefit ratio was questioned, the Committee voted unanimously to approve it.

We learned that waivers had been granted to individuals who had financial ties to the industry. This is troubling. At the time the Rotashield vaccine was approved and recommended for universal use, the following conditions existed: (1) That members, including the chair, of the FDA and CDC advisory committees who make these decisions own stock in drug companies that make vaccines. (2) That individuals on both advisory committees own patents for vaccines under consideration or affected by the decisions of the committee.  (3) That three out of five of the members of the FDA’s advisory committee who voted for the rotavirus vaccine had conflicts of interest that were waived. (4) That seven individuals of the 15 member FDA advisory committee were not present at the meeting, two others were excluded from the vote, and the remaining five were joined by fivetemporary voting members who all voted to license the product. (5) That the CDC grants conflict-of-interest waivers to every member of their advisory committee a year at a time, and allows full participation in the discussions leading up to a vote by every member, whether they have a financial stake in the decision or not. (6)

 

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