Page 78 - Fall2020

Deisher states, was recorded on video falsely claiming that To illustrate the autoimmune capability of
“Anyone who vaccines are not made from aborted fetal cells, even tiny amounts of DNA residue, Deisher’s
and he also insists that vaccines do not contain letter explains how fetal DNA sets a pregnant
says that the mercury. (Information on the CDC’s website mother’s labor into motion: “[L]abor is trig-
33
fetal DNA shows that both of Pan’s claims are blatantly gered by fetal DNA from the baby that builds
contaminating false. 34,35 ) up in the mother’s bloodstream, triggering a
massive immune rejection of the baby. This is
our vaccines DNA CONTAMINATION labor.” But whereas labor is a “naturally desired
is harmless In addition to ethical concerns, there are autoimmune reaction,” the same cannot be said
either does serious health ramifications associated with of the childhood autoimmunity that alarm-
using aborted fetal cell lines to make vaccines ingly can result from injection with fetal-cell-
not know because every single vaccine produced in this manufactured vaccines. Deisher states, “Anyone
anything manner contains DNA contaminants. According who says that the fetal DNA contaminating

about to the biomedical research entity Sound Choice our vaccines is harmless either does not know
Pharmaceutical Institute (SCPI), a total of twen-
anything about immunity and toll-like recep-
immunity ty-four vaccines are produced using cells from tors or they are not telling the truth.” Deisher
and toll-like aborted fetuses and/or contain DNA, proteins or also firmly reiterates, “If fetal DNA can trigger

receptors related cellular debris from cell cultures derived labor. . . then those same levels in vaccines can
from aborted human fetuses. Ten of these trigger autoimmunity in a child,” concluding
36
or they are vaccines are regularly used in America. Vac- that “This is direct biological evidence that
37
not telling cines identify these sources of human proteins fetal DNA contaminants in vaccines are not in
the truth.” as human albumin derived from human blood low innocuous amounts” but are “a very strong
or genetically engineered human albumin made proinflammatory trigger.”
38
from yeast, but vaccine package inserts do not In her letter, Dr. Deisher writes that inject-
contain any information about where the human ing children with human fetal DNA contami-
blood is obtained. In addition to vaccines, there nants not only runs the risk of causing the im-
are currently three FDA-approved recombinant mune system of genetically susceptible children
drugs (with up to eighty-five more coming soon) to attack their own body, leading to autoimmune
that are produced using human fetal cell lines disease, but also introduces the frightening po-
or proteins. tential for “insertional mutagenesis,” because
23
Dr. Theresa Deisher is the founder and lead the fetal DNA contaminants are the “perfect
scientist at SCPI, whose mission is “to educate size” to incorporate into a child’s own DNA and
the public about vaccine safety, as well as to cause mutations. Deisher cites gene therapy
38
pressure manufacturers to provide better and experiments in mice which demonstrated that
safer vaccines.” Deisher obtained her PhD in very low levels of DNA fragments resulted in
38
molecular and cellular physiology from Stanford insertional mutagenesis in 100 percent of the
University and has spent over twenty years in mice injected. The levels of human fetal DNA
commercial biotechnology. fragments to which children are exposed from
In an April 2019 “open letter to legislators the MMR-II as well as vaccines for chickenpox
regarding fetal cell DNA in vaccines,” Deisher and hepatitis A are far higher than the low levels
describes the problem of DNA contaminants that produced these results in mice.
in Merck’s MMR-II vaccine, reporting that its A third concern identified by Deisher is
production process results in a vaccine that is retrovirus contamination. Deisher cites a ret-
heavily contaminated with human fetal cell rovirus called human endogenous retrovirus K
DNA. Her studies have revealed that the levels (HERVK) as a known contaminant in the MMR
of fetal DNA in MMR-vaccinated children have vaccine, while pointing to research showing
the potential to incite autoimmunity in suscep- HERVK’s potential to be “reactivated” in hu-
tible children through overactivation of toll-like mans 39,40 and its association with autoimmune
receptors (receptors that play a key role in the disease. 41,42 She also notes that HERVK is in
innate immune system). 38 the same family as another retrovirus used in a
76 Wise Traditions FALL 2020