Fw: Aborted Fetal DNA/Autism

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"Do not fear nor be dismayed for the Lord your God is with you ALWAYS!" 1:9 "The mighty oak was once a NUT that stood it's ground."Tuesday July 21, 2009Is Aborted Fetal DNA in Vaccines Linked to Autism?TODAY'S HEADLINES | SEND NEWS TIPS | DONATESHARE: E-MAIL PRINT By Theresa A. Deisher, Ph.D.July

21, 2009 (LifeSiteNews.com) - 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. 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

(SCPI), 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 Biotechnology Company (www.avmbiotech.com),

which promote pro-life biotechnology. This article is an adaptation and

update of SCPI's June 2009 newsletter and is published with its kind

permission.)"Do not fear nor be dismayed for the Lord your God is with you ALWAYS!" 1:9 "The mighty oak was once a NUT that stood it's ground."Protect yourself from radiation and Bring your body back into balance... http://www.cellphoneguardian.com/cmd.php?af=731322