Posted on 07/21/2009 2:33:29 PM PDT by Maigret
IS ABORTED FETAL DNA LINKED TO AUTISM?
By Theresa A. Deisher, Ph.D.
Just when the pharmaceutical industry thought the vaccine-autism controversy had been resolved, the National Vaccine Advisory Committee has recommended further study of vaccine safety. A perceived fear of the safety of the U.S. vaccination schedule has led increasing numbers of parents to opt out of full compliance. The numbers of children who are not fully vaccinated has now reached a point where “herd” immunity may be compromised, compelling the Centers for Disease Control to hold town-hall meetings and convene a Vaccine Safety Working Subgroup. Despite research ruling out mercury (Thimerosal) or the measles portion of one specific vaccine, autism continues to rise to a level of one in every 64 children in the UK.
The NVAC draft report recommends further study of the potential for vaccines to contribute to autism in children who have underlying mitochondrial disease, a worthwhile study given the clinical history of such children developing autism after vaccinations (see Poling case). What the NVAC has overlooked, however, in their recommendations, is that epidemic regressive autism is associated with the switch from using animal cells to produce vaccines to the use of aborted human fetal cells for vaccine production. Now when we vaccinate our children, some vaccines also deliver contaminating aborted human fetal DNA. The safety of this has never been tested.
Autism and autism spectrum disorder are polygenic diseases, meaning that multiple genes have been shown to be associated with these diseases. Studies have also clearly shown that there is an environmental component, a trigger, that is required. Vaccines are an obvious potential environmental trigger for autism because of the almost universal childhood exposure to vaccines in first world countries. The vaccine-autism connection was first hypothesized following the introduction of a new measles, mumps and rubella (MMR) vaccine to the U.S. in 1979, with complete U.S. market share by 1983, and to the UK in 1988. Autism rates began to rise in the U.S. after 1979 and rose dramatically after 1983, and likewise rose in the UK after 1988, leading physicians to suspect a link. Initially, the measles component of this vaccine, MMR II, was suspected to be the culprit. Subsequent studies have also focused on the presence of mercury in vaccines, which incidentally, the MMR II vaccine did not contain.
Those studies have largely ruled out the new measles portion of the MMR II or mercury as the environmental trigger for autism. However, the compelling temporal association between this new MMR vaccine and autism cannot be ignored or explained away. What has been ignored is the fact that this new MMR vaccine introduced the use of aborted fetal cells for vaccine production. At one point, as much as 94 percent of children in the U.S. and 98 percent of children in the UK were given this vaccine.
Today, more than 23 vaccines are contaminated by the use of aborted fetal cells. There is no law that requires that consumers be informed that some vaccines are made using aborted fetal cells and contain residual aborted fetal DNA. While newer vaccines produced using aborted fetal cells do inform consumers, in their package inserts, that the vaccines contain contaminating DNA from the cell used to produce the vaccine, they do not identify the cells as being derived from electively aborted human fetuses. (See the Varivax—chicken pox—package insert for the presence of MRC5 residual DNA.)
In other words, they tell you what is in the vaccine, but they don’t fully inform you where it came from. The earliest aborted fetal cell-produced vaccines such as Meruvax (rubella) and MMR II do not even inform consumers that the vaccines contain contaminating DNA from the cell used to produce them. Furthermore, it is unconscionable that the public-health risk of injecting our children with residual contaminating human aborted fetal DNA has been ignored.
How could the contaminating aborted fetal DNA create problems? It creates the potential for autoimmune responses and/or inappropriate insertion into our own genomes through a process called recombination. There are groups researching the potential link between this DNA and autoimmune diseases such as juvenile (type I) diabetes, multiple sclerosis and lupus. Our organization, Sound Choice Pharmaceutical Institute, is focused on studying the quantity, characteristics and genomic recombination of the aborted fetal DNA found in many of our vaccines.
Preliminary bioinformatics research conducted at SCPI indicates that “hot spots” for DNA recombination are found in nine autism-associated genes present on the X chromosome. These nine genes are involved in nerve-cell synapse formation, central nervous system development and mitochondrial function.
Could genomic insertion of the aborted fetal DNA, found in some of our childhood vaccines since 1979, be an environmental trigger for autism? Could the fact that genes critical for nerve synapse formation and nervous system development are found on the X chromosome provide some explanation of why autism is predominantly a disease found in boys? Could the “hot spots” identified in these autism-associated genes be sites for insertion of contaminating aborted fetal DNA?
These questions must be answered, and quickly. Recent literature suggests that autism spectrum disorder may now impact one out of every 100 children. The pharmaceutical industry is also currently moving to replace more animal-produced vaccines with aborted-fetal-cell production and also to produce biologic drugs using aborted fetal cells.
The practice of using aborted fetal cells for vaccine and drug production creates wrenching moral dilemmas for parents and consumers, ignores informed consent rights, and exposes our children and ourselves to contaminants lacking safety evaluations. We cannot ignore this issue in good conscience, and we cannot afford to wait.
Dr. Deisher is president of Sound Choice Pharmaceutical Institute (www.soundchoice.org), as well as a cofounder and the research and development director for Ave Maria Biotechnology Company (www.avmbiotech.com), which promote pro-life biotechnology. This article is an adaptation and update of Sound Choice Pharmaceutical Institute’s June 2009 newsletter and is published with its kind permission. For more information on Dr. Deisher, see "Providing real choice: A conversation with Dr. Theresa Deisher" in American Life League's Celebrate Life magazine (January-February 2009) .
I’m disgusted to think that my daughter may have received aborted fetal cells in her various shots. Horrified actually.
Forget trying to talk these nut balls out of their conspiracies, they don’t listen to reason. 9/11 was a US plot, we didn’t land on the moon, et al; you can not convince them no mater how much evidence you post that the original study that all this vaccine cr@p is based off of was bad research done by someone with an agenda.
Facts make no difference to them, it’s about feelings, not facts, and they “feel” that somebody must be to blame for their baby’s problems and they can not accept that stuff just happens.
This is not to say that all people with autistic kids feel this way, I have an autistic nephew, sweetest kid in the world, and his parents do not buy into this crap, they just love and accept him for who he is and are not looking for someone to blame.
Having read #7, I’ll reserve judgement until I get home to read some more sources. Any links of repute are appreciated.
Read post #7, she didn’t.
sorry, you saw it first
US AND CANADA - ABORTED FETAL CELL LINE PRODUCTS AND ETHICAL ALTERNATIVES
http://www.cogforlife.org/fetalvaccines.htm
these vaccines were made originally in 1979.
The “upsurge” in autism comes much much later: in the 1990’s.
This is anti vaccine propaganda by people who have never seen an child born deaf and autistic from rubella, have never seen children die of measles, or a child who ends up with brain damage from whooping cough.
The rubella vaccine used virus from fetuses aborted for deformities but that was many years ago, and I’m not sure that thirty years later there is a lot of fetal DNA still around...
So the vaccines were not made from fetuses aborted to make vaccine (as is implied in the article). Before Roe V Wade, abortions for rubella infection was allowed, because of the terrible damage to the child (retardation, autism, blindness, deafness).
And the Vatican, when asked, said that since the cooperation with evil was limited and remote there was no alternative, that the vaccine could be used by Catholics until another vaccine was devised.
The spike on cases could be now due to the fact that doctors now know what to look for. Also there is also the possibility of overdiagnosis.
Shame on this “doctor” and shame on you for publishing it.
If someone who reads this doesn’t vaccinate his or her kids, and they end up sick or brain damaged or dead, you are partly responsible for it.
And why not suspect chemicals in the environment that could cause subtle brain damage? This could explain why I saw a lot of autism in Boston, but I rarely saw any on the Indian reservations.
Having a “retarded” child is a shame to the parents, but if they call the kid “autistic”, they can ignore his retardation, and all the social stigma that goes along with it.
But 30 years ago, I worked in an institution for the retarded, and many of our moderate and profoundly retarded had “autistic” behavior...but did not have that diagnosis on their charts.
Children with Down’s syndrome have normal behavior, as do children with myelomeningocoel and mild retardation.
But children who suffered interuterine infections (rubella, cytomegalovirus) or interuterine hypoxia (toxemia/pre eclampsia/hypertension) or who were born prematurely who in the past would have died now are living at home, and some of them have subtle brain damage.
But many of those who fit the classic “autism” syndrome include autistic children who have a history of such infections, or suffered from Fragile X syndrome.
Autism has increased in diagnosis, simply because the definition of autism was nailed down, and because government funding for special ed is linked to a positive diagnosis of Autism.
The same is true of Multiple Sclerosis for which there was no clear set of standards before the McDonold criteria accepted in 2001.
Although the McDonald Criteria and the 911 attacks both have an “undeniable temporal link” I want someone to sell me the connection between Multiple Sclerosis and the 911 attacks.
This article is full of broad strokes, also known as BS.
Incessant crying. Inability to process and synthesize visual information. How could I tell that with a 10-day old baby, my first child? I just could. Mother’s instinct.
When he was about 18 months to 2 years old, and we could communicate some - he could understand, but not speak, could use a little sign language - it was very clear that he saw the world in unrelated fragments.
He’s come a long long way, but he still has some problems with conceptual and physical synthesis.
bookmark
I didn’t.
OMGOSH.”Now when we vaccinate our children, some vaccines also deliver contaminating aborted human fetal DNA”
My opinion is that the uptick in Autism is caused by VCRs and DVDs.
Stick a kid in front of a tv and never talk to him, then see what happens.
That and “Autism Spectrum” gets more money for schools. Many “High energy” kids are now diagnosed in the “Autism spectrum”. In fact, we camped with friends who told us that their 11 year old was Autistic, when he had never been diagnosed at all.
Does the author of this article *know* this? There’s a good deal of speculation and no facts. This isn’t even a hypothesis to test upon.
I have a niece who has Asperger’s syndrome and my future son-in-law is a very functional autistic. It's partially genetic, but there has to be some environmental trigger too.
I've known it for years, and it is why NONE of my five children have had ANY vaccinations. ( my oldest daughter did get two MMR shots before I started reading two years ago) but I have kept my kids away from the needles and the mercury and the aborted fetal tissue and the other toxic ingredients, and guess what?
None of them is autistic.
Jenny
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