Vaccines laced with aborted fetal tissue since 1979
Dec 09, 2016
The Laws of Tribulation in Deuteronomy 28:57 says that if we persist in violating the laws of God, we will eat our children. In ancient times, a siege on a city could result in such a severe shortage of food that this would actually happen. Such an example is seen in the Syrian siege of Samaria in 2 Kings 6:28, 29.
Eating human flesh has gone on for a long time in various primitive cultures, and it has also persisted in various Satanist groups in Western countries. But because we have violated the divine law, the vast majority of westerners have inadvertently “eaten” their children through the use of vaccines. In 1973 abortion was legalized in the USA, and in 1979 pharmaceutical companies began to use aborted fetal tissue in their vaccines.
In doing so, everyone receiving a vaccine (or perhaps certain common vaccines) are “eating” the aborted remains of aborted children. In 1988 they started putting mercury poisons (thimerosol) into vaccines for no good reason except to keep the vaccine “fresh.” (In my view they were really looking to increase their profits by making more people sick with new diseases, so that they could develop more vaccines for those new diseases.) In doing so, we have greatly increased autism in children, a condition that was rare prior to 1979.
In 1979 we started injecting our children with vaccines that are contaminated with human fetal DNA fragments and a retrovirus, and autism began to rise. Then we added more jabs with aborted fetal vaccines and thimerosal, which can also cause DNA breaks, to vaccines in 1988, and autism rose more. Then in 1995, we added much more aborted fetal DNA contaminants to the chickenpox vaccine, and autism really rose. And now we have children born to older dads who have sperm with very breakable DNA. Aborted fetal contaminated vaccines plus thimerosal plus older dads result in more DNA breaks, thus more de novo mutations, in our children.
Drugs and vaccines are too large to produce in a test tube, and therefore, they must be manufactured using cell lines. The final products contain contaminants from the cell line used to manufacture the drug or vaccine. When animal cell lines are utilized, these contaminants are recognized by our immune systems as ‘foreign’ and are eliminated from our bodies. However, when primitive human cell lines (such as an aborted fetal cell line) are used, these contaminants have the potential to trigger autoimmune diseases or genomic instability. When we use human fetal produced vaccines or cosmetics, we are also injecting or transferring DNA and viruses from the human fetus used to create the cell line into our own bodies.
Of course, participating in the judgment of God, as specified in the Law of Tribulation, is applied under a wooden yoke, rather than under an iron yoke. That makes it voluntary… at least, so far. But now there are new laws being passed to make such vaccines mandatory. We are dangerously close to coming under an iron yoke (Deuteronomy 28:48). I do not think that this will happen, at least not on a large scale, but rather it tells me that we are nearing the end of the wooden yoke captivity that began in 1913-1914 with the establishment of the Federal Reserve Bank.
An article from Sound Choice Pharmaceutical Institute reads,
The potential consequences of injecting our children with human fetal DNA contaminants include two well-established pathologies:
1) Autoimmune disease triggered by the human fetal DNA in vaccines leading a child’s immune system to attack his or her own body, and
2) Insertional mutagenesis in which fetal DNA incorporates into the child’s DNA causing mutations. Scientists have found that children with autistic disorder have antibodies against human DNA in their blood that non-autistic children do not have. These antibodies may be involved in autoimmune attacks in autistic children. Scientists have also found that autistic children have hundreds of excess rare, de novo mutations….
Fetal Vaccines and Childhood Cancers
At the 2009 Washington State Medical Association Annual Conference a prominent pediatric oncologist shared her concerns that the MMR II vaccine was associated with rising and alarming childhood leukemias and lymphomas. As a small non-profit, SCPI has been forced to focus solely on fetal vaccines and autism, however, in May 2014 we made investigating childhood cancers and their relationship to fetal manufactured vaccines one of our annual goals.
How ironic then that Dr. Deisher’s son Henry was diagnosed with very aggressive lymphoma on July 30, 2014. Not knowing the human fetal source of some vaccines, Dr. Deisher’s children received several fetal vaccines as infants and toddlers. Henry was injected with fetal contaminated vaccines as a toddler, yet the cancer did not rear its ugly head until he was 13.
The article is not long, but it is very informative and professional.
Dr. Stephen Jones